Cook
Flexible Stylet For Removal of 14FR Malecot Nephrostomy Catheter
1manufacturer
35catalogue numbers in this listing
3510(k) clearances naming this product code
4recalls on this code
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Well Lead Medical Co., Ltd. | Guangzhou | Guangdong | Contract manufacturer | 46 |
Record
| Listed by | Cook Incorporated, United States |
|---|---|
| FDA product code | KOB |
| Device type | Catheter, Suprapubic (And Accessories) |
| Device class | Class 2 |
| Regulation | 21 CFR 876.5090 |
| Establishment | Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K182709 |
| Record published | 2015-10-24 |
| Record revised | 2024-05-16 (version 4) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Storage | Special storage condition: Store in dark, dry, cool place. |
| Distribution end date | 2017-08-24 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| G14899 | In distribution | |
| G17239 | In distribution | |
| G14227 | In distribution | |
| G14496 | In distribution | |
| G14161 | In distribution | |
| G26666 | In distribution | |
| G25981 | In distribution | |
| G14228 | In distribution | |
| G14097 | In distribution | |
| G26642 | In distribution | |
| G14329 | In distribution | |
| G19087 | In distribution | |
| G14094 | In distribution | |
| G26648 | In distribution | |
| G16699 | In distribution | |
| G19091 | In distribution | |
| G14764 | In distribution | |
| G15469 | In distribution | |
| G26655 | In distribution | |
| G16696 | In distribution | |
| G14495 | In distribution | |
| G14234 | In distribution | |
| G14490 | In distribution | |
| G15819 | In distribution | |
| G19089 | In distribution | |
| G14210 | In distribution | |
| G14095 | In distribution | |
| G14182 | In distribution | |
| G16740 | In distribution | |
| G16697 | Withdrawn | |
| G16791 | Withdrawn | |
| G16741 | Withdrawn | |
| G16700 | Withdrawn | |
| G14183 | Withdrawn | |
| G17515 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| MiniSPC Button | Applied Medical Technology, Inc. | 284 |
| Malecot | Cook Incorporated | 39 |
| Stamey | Cook Incorporated | 16 |
| Silicone Supra-Pubic Catheter (Ordinary Balloon) | Fortune Medical Instrument Corp. | 10 |
| Rutner | Cook Incorporated | 9 |
| Silicone Supra-Pubic Catheter (Integrated Balloon) | Fortune Medical Instrument Corp. | 8 |
| Cook-Cope Loop | Cook Incorporated | 8 |
| Silicone Supra-Pubic Catheter Exchange Set (Ordinary Balloon) | Fortune Medical Instrument Corp. | 7 |
| S-Cath™ | Mediplus Ltd. | 7 |
| Silicone Supra-Pubic Catheter Exchange Set (Integrated Balloon) | Fortune Medical Instrument Corp. | 7 |
| Mediplus | Mediplus Ltd. | 6 |
| AMT MiniSPC Drainage Set | Applied Medical Technology, Inc. | 6 |
Showing 12 of 23. All products under Catheter, Suprapubic (And Accessories)
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K181097 | 2019-01-18 |
| K182709 | 2018-12-26 |
| K182066 | 2018-10-30 |
Recalls
4 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2019-04-22 | Class II | Error in labeling | Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting. | 3711 | 2020-05-05 |
| 2019-04-22 | Class II | Error in labeling | Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting. | 12968 | 2020-05-05 |
| 2019-01-04 | Class II | Process control | The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip. | 13388 total | 2020-05-29 |
| 2019-01-04 | Class II | Process control | The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip. | 13388 total | 2020-05-29 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.