Primeline Medical Products, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Primeline Medical Products, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Primeline Medical Products, Inc. has 9 FDA 510(k) cleared medical devices. Based in Edmonton, Alberta, CA.
Historical record: 9 cleared submissions from 1997 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Primeline Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Primeline Medical Products, Inc.
9 devices
Cleared
Nov 08, 2002
PRIMAGARD SURGICAL EQUIPMENT DRAPES
General Hospital
71d
Cleared
Nov 08, 2002
PRIMAGARD SURGICAL GOWNS
General Hospital
58d
Cleared
Nov 08, 2002
PRIMAGARD SURGICAL GOWNS
General Hospital
39d
Cleared
Sep 23, 2002
PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119,...
General Hospital
109d
Cleared
Apr 16, 2002
PRIMAGARD YELLOW SURGICAL MASK, PLEATED, TIE-ON, PM4-307
General Hospital
13d
Cleared
Jun 22, 2001
PROCEDURE MASKS: PM4-301 AND PM4-304
General Hospital
14d
Cleared
Sep 08, 2000
PRIMED PLEATED TIE-BACK, PROCEDURE MASK PM4-305, PRIMED PLEATED EAR-LOOP,...
General Hospital
73d
Cleared
Jan 13, 1998
PRIMED SHOE COVERS, PRIMED HEAD COVERS
General Hospital
295d
Cleared
Jun 22, 1997
PRIMED PRIME-PLUS COTTON GAUZE SPONGES
General & Plastic Surgery
90d