Smith & Nephew United, Inc.
FDA 510(k) & PMA Approved Devices — 34 products
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Total Devices34
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K963096 | ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING | KMF | 1996-10-25 | View |
| 510(k) | K961775 | PROFORE FOUR-LAYER BANDAGE SYSTEM KIT | EFQ | 1996-07-16 | View |
| 510(k) | K945330 | ALLEVYN ADHESIVE | KMF | 1995-02-09 | View |
| 510(k) | K943619 | CAVI-CARE CONFORMING FOAM DRESSING | KMF | 1994-08-19 | View |
| 510(k) | K942748 | INTRASITE | NAE | 1994-06-29 | View |
| 510(k) | K935705 | ALLEVYN ISLAND WOUND DRESSING | NAE | 1994-02-15 | View |
| 510(k) | K935803 | CICA-CARE SILICONE GEL SHEET | MDA | 1994-02-03 | View |
| 510(k) | K932263 | SOLOSITE DERMAL WOUND GEL | MGQ | 1993-10-01 | View |
| 510(k) | K926508 | INTRASITE GEL | NAE | 1993-07-13 | View |
| 510(k) | K922897 | STRAPPAL | KGX | 1992-09-15 | View |
| 510(k) | K914147 | ALLEVLYN WOUND DRESSING, MODIFICATION | KMF | 1992-02-03 | View |
| 510(k) | K915150 | REMOVE ADHESIVE REMOVER | KOX | 1992-01-09 | View |
| 510(k) | K911682 | AIRSTRIP FIRST AID & POST-OP DRESSING | KGX | 1991-07-17 | View |
| 510(k) | K911660 | INTRASITE HYDROCOLLOID WOUND DRESSING | MGP | 1991-06-17 | View |
| 510(k) | K904411 | INTRASITE GEL (LABELING REVISION) | KMF | 1990-11-26 | View |
| 510(k) | K904412 | ALLEVYN DRESSING CLAIMS CHANGE | KOZ | 1990-10-23 | View |
| 510(k) | K901876 | INTRASITE CAVITY WOUND DRESSING (LABEL REVISION) | KOZ | 1990-06-28 | View |
| 510(k) | K901878 | INTRASITE GEL (LABELING REVISION) | KMF | 1990-06-22 | View |
| 510(k) | K901877 | ALLEVYN DRESSING (LABELING REVISED) | KMF | 1990-06-22 | View |
| 510(k) | K901879 | INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING) | KGX | 1990-06-22 | View |
No matching devices.
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