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) cleared devices by 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