Primeline Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K022868 | PRIMAGARD SURGICAL EQUIPMENT DRAPES | November 8, 2002 |
| K023266 | PRIMAGARD SURGICAL GOWNS | November 8, 2002 |
| K023117 | PRIMAGARD SURGICAL GOWNS | November 8, 2002 |
| K021864 | PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119, PM1-0142) | September 23, 2002 |
| K021076 | PRIMAGARD YELLOW SURGICAL MASK, PLEATED, TIE-ON, PM4-307; PRIMAGARD YELLOW SURGICAL MASK, PLEATED, E | April 16, 2002 |
| K011789 | PROCEDURE MASKS: PM4-301 AND PM4-304 | June 22, 2001 |
| K001951 | PRIMED PLEATED TIE-BACK, PROCEDURE MASK PM4-305, PRIMED PLEATED EAR-LOOP, PROCEDURE MASK PM4-306 | September 8, 2000 |
| K971076 | PRIMED SHOE COVERS, PRIMED HEAD COVERS | January 13, 1998 |
| K971075 | PRIMED PRIME-PLUS COTTON GAUZE SPONGES | June 22, 1997 |