Professional Medical Services
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 19
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K913094 | DISPOSABLE SLIDE VALVE MANIFOLD | January 27, 1992 |
| K910378 | PRESSURE MONITORING EXTENSION LINE | April 22, 1991 |
| K904508 | CONDOR ANALOG INFLATION SYRINGE | April 2, 1991 |
| K904954 | CONDOR DIGITAL INFLATION SYRINGE | January 16, 1991 |
| K902606 | RADIOPAQUE RULER | September 27, 1990 |
| K884577 | PROCEDURE READY TRAYS | August 1, 1989 |
| K890471 | PMS ANGIO DRAPE | February 27, 1989 |
| K884497 | CONTROL SYRINGE | December 12, 1988 |
| K872448 | BLOOD CONTAINMENT PACK | November 17, 1987 |
| K864555 | 3 RING ATTACHMENT | December 1, 1986 |
| K854941 | PMS PERCUTANEOUS PUNCTURE NEEDLE | April 16, 1986 |
| K850632 | PMS AMNIOCENTESIS TRAY/KIT | May 22, 1985 |
| K850050 | PMS OPHTHALMOLOGY PACK-PMS EYE TRAY/PACK | April 23, 1985 |
| K844465 | PMS DRAPE PACK | December 5, 1984 |
| K842149 | PMS SUTURE PACK/TRAY;VERTEX SUTURE | July 23, 1984 |
| K841468 | PMA ANGIOGRAPHY TRAY | June 5, 1984 |
| K840671 | CARDIAC CATHETERIZATION PACK | March 12, 1984 |
| K840017 | VERTEX PERCUTANEOUS CATHETER INTRODUC | February 4, 1984 |
| K830637 | VERTEX DIGITAL SUBSTRATION KIT | March 24, 1983 |