7 catalogue numbers from 4890-8218, listed by Fortune Medical Instrument Corp., Taiwan, under Catheter, Suprapubic (And Accessories). 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Silicone Supra-Pubic Catheter Exchange Set (Integrated Balloon) | Listed by | Fortune Medical Instrument Corp., Taiwan |
| FDA product code | KOB |
| Device type | Catheter, Suprapubic (And Accessories) |
| Device class | Class 2 |
| Regulation | 21 CFR 876.5090 |
| Establishment | Contract manufacturer, Manufacturer |
| 510(k) | K014002 |
| Record published | 2016-03-11 |
| Record revised | 2024-05-16 (version 4) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, manufacturing date |
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.