Johnson & Johnson Medical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 56
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K033523 | COLLAGEN-ORC ANTIMICROBIAL MATRIX | October 21, 2004 |
| K022483 | ACTISORB SILVER 220 ANTIMICROBIAL BINDING DRESSING | February 3, 2003 |
| K014129 | PROMOGRAN MATRIX WOUND DRESSING | February 14, 2002 |
| K001690 | PROTECTIV SAFETY BLOOD COLLECTION NEEDLE | July 31, 2000 |
| K982641 | ADVANCED NIBP MODULE | March 29, 1999 |
| K983362 | NU-GEL * WOUND DRESSING | December 16, 1998 |
| K982597 | FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATE | August 20, 1998 |
| K974080 | CRITIKON SOFT BLOOD PRESSURE CUFF | May 18, 1998 |
| K980493 | I.V. CATHETER SYSTEM | April 28, 1998 |
| K972498 | OBSERVER * CENTRAL STATION | February 17, 1998 |
| K973699 | ULTRALON POWDER FREE LATEX SURGICAL GLOVE | December 16, 1997 |
| K971569 | DINAMAP MPS PORTABLE MONITOR | September 19, 1997 |
| K970182 | DINAMAP COMPACT MONITOR | August 18, 1997 |
| K964556 | HR POLYURETHANE PICC AND MIDLINE CATHETERS | April 16, 1997 |
| K970721 | DYNA-FLEX MULTI-LAYER COMPRESSION SYSTEM | March 21, 1997 |
| K965040 | INTROL BLADDER NECK SUPPORT PROSTHESIS WITH REMOVAL TOOL | March 10, 1997 |
| K962978 | CCENTERMARK CATHETER INTRODUCER SHEALTH WITH PROTECTIV 2000 NEEDLE SAFETY SYSTEM | January 7, 1997 |
| K964016 | TIELLE HYDROPOLYMER FOAM DRESSING | December 31, 1996 |
| K962226 | PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM | December 23, 1996 |
| K962986 | MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES | September 20, 1996 |