FDA Product Code
FDA Product Code DQI — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Cardiovascular
- 21 CFR Citation
- 870.1800
510(k) Clearances — 9 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K960486 | KSEA MODEL 383320 20 ANGIOMAT | Karl Storz Endoscopy | 1996-10-25 | Traditional | PDF ↗ |
| K935763 | SURGIPUMP | W.O.M. World of Medicine GmbH | 1994-04-21 | Traditional | PDF ↗ |
| K922541 | USCI SUPER 9 PTCA GUIDING CATHETER | C.R. Bard, Inc. | 1992-12-08 | Traditional | PDF ↗ |
| K924110 | LEOCOR CORFLO PUMP -- MODIFICATION | Leocor, Inc. | 1992-09-01 | Traditional | PDF ↗ |
| K905189 | BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL) | Baxter Healthcare Corp | 1991-01-30 | Traditional | PDF ↗ |
| K902444 | CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP | Intramed Laboratories, Inc. | 1990-08-30 | Traditional | PDF ↗ |
| K895688 | NOBLES-LAI ENGINEERING INFUSION PUMP | Nobles-Lai Engineering, Inc. | 1990-02-26 | Traditional | PDF ↗ |
| K895074 | ANGIOSCOPY PUMP | Baxter Healthcare Corp | 1990-01-31 | Traditional | PDF ↗ |
| K871422 | OLYMPUS ANGIOSCOPY PUMP | Olympus Corp. | 1987-08-12 | Traditional | PDF ↗ |
Product code DQI · Class II · Cardiovascular. Data: openFDA.