American Convertors Div., American Pharmaseal is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Convertors Div., American Pharmaseal - FDA 510(k) Cleared De...
19
Total
19
Cleared
0
Denied
American Convertors Div., American Pharmaseal has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1980 to 1984. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by American Convertors Div., American Pharmaseal Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Convertors Div., American Pharmaseal
19 devices
Cleared
Jun 07, 1984
ANTIMICROBIAL INCISE DRAPE
General Hospital
93d
Cleared
Aug 12, 1983
CONVERTORS FLASH STERILIZING TRAY
General & Plastic Surgery
42d
Cleared
May 18, 1983
DISIMETRIC RELEASE OF INSTRANETICS RAD
Gastroenterology & Urology
68d
Cleared
May 13, 1982
ABSORB FURN SHEET
General & Plastic Surgery
35d
Cleared
Jan 22, 1982
COMFORT CUSHION DRY BURN PAD III
General & Plastic Surgery
46d
Cleared
Dec 29, 1981
CONVERTORS STERILE DISP. LAP SPONGE II
General & Plastic Surgery
36d
Cleared
Dec 18, 1981
CONTURA DISPOS. SURG. FACE MASK
General Hospital
46d
Cleared
Sep 24, 1981
TOMAC STERILE DISP. LAP SPONGE
General & Plastic Surgery
16d
Cleared
Feb 02, 1981
ISO-BAC INSTRUMENT WRAP
General Hospital
76d
Cleared
Dec 22, 1980
PATIENT CARE DISPOSABLE INFANT SHIRTS
General Hospital
27d
Cleared
Oct 31, 1980
COMFORT CUSHION DRY BURN PADS, STERILE
General Hospital
38d
Cleared
Oct 31, 1980
DISP. FENESTRATED SURG. DRAPE SHEETS
General Hospital
35d