Medical Device Manufacturer · US , Mchenry , IL

Bemis Health Care - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1976

Total

Cleared

Denied

Bemis Health Care has 12 FDA 510(k) cleared general hospital devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1976 to 1989.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

Bemis Health Care 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 - Bemis Health Care

12 devices

1-12 of 12

Cleared Jan 25, 1989

BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.

K885019 · FRG

General Hospital · 57d

Cleared Oct 18, 1982

CRITICAL MEASUREMENT UNIT

K822556 · BYZ

General Hospital · 55d

Cleared Oct 18, 1982

SPECIMEN ADAPTOR

K822557 · BYZ

General Hospital · 55d

Cleared Jan 21, 1981

SUCTION PROBE

K803206 · JOL

General Hospital · 35d

Cleared Dec 20, 1977

SUCTION CANISTER

K771737 · GCX

General Hospital · 96d

Cleared Sep 28, 1977

8 EMESIS BASIN

K771733 · FNY

General Hospital · 13d

Cleared Sep 28, 1977

MALE URINAL

K771738 · FNP

General Hospital · 13d

Cleared Aug 23, 1976

BED PAN, STACKABLE (AUTOCLAVABLE)

K760393 · FOB

General Hospital · 17d

Cleared Jul 20, 1976

TUMBLER, PERSONAL, ROUND, 9 OUNCE

K760070

General Hospital · 32d

Cleared Jul 20, 1976

TRAY, PERSONAL, RECTANG. 8 1/2 X 5 1/4

K760071

General Hospital · 32d

Cleared Jul 20, 1976

CARAFE, PERSONAL, 1-QT SEMI-RECTANGULAR

K760072

General Hospital · 32d

Cleared Jul 20, 1976

BASIN, WASH, 6-QT RECTANGULAR

K760073 · LDQ

General & Plastic Surgery · 32d

Bemis Health Care - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Bemis Health Care

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