FDA 510(k) Applications Submitted by PRIMELINE MEDICAL PRODUCTS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K023117 |
09/11/2002 |
PRIMAGARD SURGICAL GOWNS |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K021076 |
04/03/2002 |
PRIMAGARD YELLOW SURGICAL MASK, PLEATED, TIE-ON, PM4-307; PRIMAGARD YELLOW SURGICAL MASK, PLEATED, EAR-LOOP,PM4-308; PRM |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K021864 |
06/06/2002 |
PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119, PM1-0142) |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K022868 |
08/29/2002 |
PRIMAGARD SURGICAL EQUIPMENT DRAPES |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K023266 |
09/30/2002 |
PRIMAGARD SURGICAL GOWNS |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K971075 |
03/24/1997 |
PRIMED PRIME-PLUS COTTON GAUZE SPONGES |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K971076 |
03/24/1997 |
PRIMED SHOE COVERS, PRIMED HEAD COVERS |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K011789 |
06/08/2001 |
PROCEDURE MASKS: PM4-301 AND PM4-304 |
PRIMELINE MEDICAL PRODUCTS, INC. |
| K001951 |
06/27/2000 |
PRIMED PLEATED TIE-BACK, PROCEDURE MASK PM4-305, PRIMED PLEATED EAR-LOOP, PROCEDURE MASK PM4-306 |
PRIMELINE MEDICAL PRODUCTS, INC. |
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