moorFLPI-2 Review PC Software
moorFLPI-2 Review PC Software V5
2manufacturers in China registered for this device type
1catalogue number
8510(k) clearances naming this product code
Who Else Makes It
All of them in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| RWD Life Science Co., Ltd. | Shenzhen | Guangdong | Manufacturer | 4 |
Record
| Listed by | Moor Instruments Ltd., United Kingdom |
|---|---|
| FDA product code | DPT |
| Device type | Probe, Blood-Flow, Extravascular |
| Device class | Class 2 |
| Regulation | 21 CFR 870.2120 |
| Establishment | Complaint-file establishment, Manufacturer |
| 510(k) | K122943 |
| Record published | 2016-11-29 |
| Record revised | 2018-07-06 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 5 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Medex | ICU Medical, Inc | 138 |
| Bio-Probe™ | Medtronic, Inc. | 21 |
| Probe, Blood-Flow, Extravascular | Medtronic, Inc. | 10 |
| Moor Instruments Ltd | Moor Instruments Ltd. | 3 |
| Trillium™ Bio-Probe® | Medtronic, Inc. | 2 |
| Trillium™ | Medtronic, Inc. | 2 |
| FloProbe 3/8’’ x 3/8” (Non Sterile) | Movair, Inc. | 1 |
| FloProbe 1/4’’ x 1/4″ (Non Sterile) | Movair, Inc. | 1 |
| FloProbe 1/4’’ x 1/4’’ (Sterile) | Movair, Inc. | 1 |
| I2P24 Doppler Probe | Deltex Medical Limited | 1 |
| I2S6 Doppler Probe | Deltex Medical Limited | 1 |
| moorFLPI2- Measurement PC Software | Moor Instruments Ltd. | 1 |
Showing 12 of 17. All products under Probe, Blood-Flow, Extravascular
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K152749 | 2016-05-12 |
| K132163 | 2014-01-29 |
| K122943 | 2013-01-03 |
| K060976 | 2007-03-27 |
| K063586 | 2007-01-25 |
| K063561 | 2007-01-19 |
| K032841 | 2003-12-10 |
| K980383 | 1998-04-30 |
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.