Johnson & Johnson Medical, Inc.
FDA 510(k) & PMA Approved Devices — 53 products
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Total Devices53
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K001690 | PROTECTIV SAFETY BLOOD COLLECTION NEEDLE | FMI | 2000-07-31 | View |
| 510(k) | K982641 | ADVANCED NIBP MODULE | DXN | 1999-03-29 | View |
| 510(k) | K983362 | NU-GEL * WOUND DRESSING | MGQ | 1998-12-16 | View |
| 510(k) | K982597 | FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATE | KGN | 1998-08-20 | View |
| 510(k) | K974080 | CRITIKON SOFT BLOOD PRESSURE CUFF | DXQ | 1998-05-18 | View |
| 510(k) | K980493 | I.V. CATHETER SYSTEM | FOZ | 1998-04-28 | View |
| 510(k) | K972498 | OBSERVER * CENTRAL STATION | DSI | 1998-02-17 | View |
| 510(k) | K973699 | ULTRALON POWDER FREE LATEX SURGICAL GLOVE | KGO | 1997-12-16 | View |
| 510(k) | K971569 | DINAMAP MPS PORTABLE MONITOR | MSX | 1997-09-19 | View |
| 510(k) | K970182 | DINAMAP COMPACT MONITOR | MHX | 1997-08-18 | View |
| 510(k) | K964556 | HR POLYURETHANE PICC AND MIDLINE CATHETERS | LJS | 1997-04-16 | View |
| 510(k) | K970721 | DYNA-FLEX MULTI-LAYER COMPRESSION SYSTEM | MCY | 1997-03-21 | View |
| 510(k) | K965040 | INTROL BLADDER NECK SUPPORT PROSTHESIS WITH REMOVAL TOOL | HHW | 1997-03-10 | View |
| 510(k) | K962978 | CCENTERMARK CATHETER INTRODUCER SHEALTH WITH PROTECTIV 2000 NEEDLE SAFETY SYSTEM | DYB | 1997-01-07 | View |
| 510(k) | K964016 | TIELLE HYDROPOLYMER FOAM DRESSING | KMF | 1996-12-31 | View |
| 510(k) | K962226 | PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM | FOZ | 1996-12-23 | View |
| 510(k) | K962986 | MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES | KGO | 1996-09-20 | View |
| 510(k) | K955113 | DINAMAP SELECT MULTI-PARAMETER SYSTEM | DPS | 1996-08-15 | View |
| 510(k) | K961632 | MICRO-TOUCH POWDER FREE LATEX SURGICAL GLOVES | KGO | 1996-07-03 | View |
| 510(k) | K944587 | DERMIVIEW HYPOALLERGENIC CLEAR TAPE | KGX | 1995-10-30 | View |
No matching devices.
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