Medical Device Manufacturer · US , Mchenry , IL

Amsco Co. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1977

Total

Cleared

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.

Amsco Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Amsco Co.

19 devices

1-12 of 19

Cleared Jun 26, 1992

EAGLE 3000 SDS

K912471 · FLE

General Hospital · 388d

Cleared Jan 24, 1986

AMSCO POLARIS SL

K854922 · FSY

General & Plastic Surgery · 45d

Cleared Oct 31, 1983

HALL OSTEON

K833187 · GET

General & Plastic Surgery · 42d

Cleared Oct 19, 1983

EAGLE 2000 STERILIZER SERIES GAS/AERA

K832945 · FLF

General Hospital · 50d

Cleared Aug 12, 1983

CEILING MOUNTED SUPPORT

K831086 · FQO

General & Plastic Surgery · 130d

Cleared Aug 12, 1983

HALL DRILL/REAMER

K832186 · GET

General & Plastic Surgery · 37d

Cleared Aug 12, 1983

HALL OSCILLATOR

K832187 · GET

General & Plastic Surgery · 37d

Cleared Aug 12, 1983

HALL RECIPROCATOR

K832188 · GET

General & Plastic Surgery · 37d

Cleared Jun 15, 1983

DELIVERY 4 TABLE

K831309 · KNC

Obstetrics & Gynecology · 54d

Cleared Dec 03, 1982

SURGICAL LIGHT

K823360 · FTD

General & Plastic Surgery · 28d

Cleared May 21, 1981

DISPOSABLE STERILIZATION WRAP

K811242 · FRG

General Hospital · 17d

Cleared Dec 11, 1980

STERNUM SAW BLADE

K802838 · GFA

General & Plastic Surgery · 29d

Amsco Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Amsco Co.

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