FDA Product Code
FDA Product Code MWI — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Cardiovascular
- 21 CFR Citation
- 870.2300
510(k) Clearances — 308 records · page 4 of 4
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K002009 | HP M2376A DEVICE LINK SYSTEM, MODEL M2376A | Agilent Technologies, Inc. | 2000-08-02 | Special | PDF ↗ |
| K001265 | WELCH ALLYN INSTRUMENT INTERFACE MODULE | Welch Allyn, Inc. | 2000-07-13 | Traditional | PDF ↗ |
| K001776 | MODIFICATION TO HP M2376A DEVICE LINK SYSTEM, MODEL M2376A | Agilent Technologies, Inc. | 2000-06-30 | Special | PDF ↗ |
| K001020 | 8100 VITAL SIGNS MONITOR | Criticare Systems, Inc. | 2000-04-28 | Special | PDF ↗ |
| K000635 | MODIFICATION TO HP M2376A DEVICE LINK SYSTEM | Agilent Technologies, Inc. | 2000-03-20 | Special | PDF ↗ |
| K992638 | DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400 | Critikon Company, LLC | 2000-02-24 | Traditional | PDF ↗ |
| K983928 | KODAK HOME HEALTH MONITORING SYSTEM | Eastman Kodak Company | 2000-02-11 | Traditional | PDF ↗ |
| K980688 | INTEGRITI PATIENT MONITOR | Alliance Instruments | 1999-03-16 | Traditional | PDF ↗ |
Product code MWI · Class II · Cardiovascular. Data: openFDA.