Amsco Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Amsco Co. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Amsco Co. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1977 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Amsco Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Amsco Co.
19 devices
Cleared
Jun 26, 1992
EAGLE 3000 SDS
General Hospital
388d
Cleared
Jan 24, 1986
AMSCO POLARIS SL
General & Plastic Surgery
45d
Cleared
Oct 31, 1983
HALL OSTEON
General & Plastic Surgery
42d
Cleared
Oct 19, 1983
EAGLE 2000 STERILIZER SERIES GAS/AERA
General Hospital
50d
Cleared
Aug 12, 1983
CEILING MOUNTED SUPPORT
General & Plastic Surgery
130d
Cleared
Aug 12, 1983
HALL DRILL/REAMER
General & Plastic Surgery
37d
Cleared
Aug 12, 1983
HALL OSCILLATOR
General & Plastic Surgery
37d
Cleared
Aug 12, 1983
HALL RECIPROCATOR
General & Plastic Surgery
37d
Cleared
Jun 15, 1983
DELIVERY 4 TABLE
Obstetrics & Gynecology
54d
Cleared
Dec 03, 1982
SURGICAL LIGHT
General & Plastic Surgery
28d
Cleared
May 21, 1981
DISPOSABLE STERILIZATION WRAP
General Hospital
17d
Cleared
Dec 11, 1980
STERNUM SAW BLADE
General & Plastic Surgery
29d
Cleared
Aug 20, 1980
STERNUM SAW
General & Plastic Surgery
26d
Cleared
May 30, 1980
PROOF (BIOLOGICAL/CHEMICAL INDICATOR)
General Hospital
18d
Cleared
Dec 28, 1978
TABLE, EXAMINING-TWO EIGHTY
Ear, Nose, Throat
15d
Cleared
May 16, 1978
MICRO RASPS
General & Plastic Surgery
11d
Cleared
Dec 08, 1977
BIOLOGICAL/CHEMICAL INDICATOR
General Hospital
24d
Cleared
Feb 28, 1977
PORTAGAS AERATOR
General Hospital
62d
Cleared
Jan 26, 1977
SURGICAL LIGHT - CHALLENGE 22 SERIES
General & Plastic Surgery
77d