American Sterilizer Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Sterilizer Co. - FDA 510(k) Cleared Devices
36
Total
35
Cleared
0
Denied
American Sterilizer Co. has 35 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 35 cleared submissions from 1977 to 1994.
Browse the FDA 510(k) cleared devices submitted by American Sterilizer Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Sterilizer Co.
36 devices
Cleared
Oct 17, 1994
AMSCO SQ240 SURGICAL LIGHT
General & Plastic Surgery
101d
Cleared
Feb 07, 1994
THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZER
General Hospital
299d
Cleared
Sep 29, 1993
CHEMDI-VHP CHEMICAL INDICATOR
General Hospital
499d
Cleared
Jun 22, 1993
QUANTUM 3080 SURGICAL TABLE
General & Plastic Surgery
141d
Cleared
Mar 06, 1991
ORTHOVISION TABLE
General & Plastic Surgery
68d
Cleared
Jan 03, 1990
AMSCO QUANTUM LIGHT
General & Plastic Surgery
37d
Cleared
Nov 17, 1989
EAGLE DS
Dental
87d
Cleared
Jul 25, 1988
GENERAL SURGICAL TABLE AND ACCESSORIES
General & Plastic Surgery
27d
Cleared
Feb 10, 1988
GEMINI SURGICAL LIGHT
General & Plastic Surgery
26d
Cleared
Dec 24, 1986
RADIOGRAPHIC - LEG SECTION
Gastroenterology & Urology
14d
Cleared
Nov 25, 1985
CHEMSPOR
General Hospital
371d
Cleared
Aug 08, 1985
AMSCO URO-ENDO MOBILE TABLE
Gastroenterology & Urology
85d