Medical Device Manufacturer · US , Mchenry , IL

Cutter Laboratories, Inc. - FDA 510(k) Cleared Devices

39 submissions · 39 cleared · Since 1976

Total

Cleared

Denied

Cutter Laboratories, Inc. has 39 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 39 cleared submissions from 1976 to 1986.

Browse the FDA 510(k) cleared devices submitted by Cutter Laboratories, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cutter Laboratories, Inc.

39 devices

1-12 of 39

Cleared May 21, 1986

HYPERBARIC PENETRATION EXTENSION SET

INTRAVENOUS INFUSION CONTROLLER

K834106 · LDR

General Hospital · 183d

Cleared Aug 16, 1983

ORTHOPEDIC CASTING TAPE MAXCAST

K832237 · ITG

Physical Medicine · 36d

Cleared Jan 12, 1983

DOSIMETRIC RELEASE PROGRAM - ADMIN. SET

K823214 · FPA

Chemistry · 76d

Cleared May 28, 1982

CUTTER BOND POLYCARBOXYLATE CEMENT

K821326 · EMA

Dental · 24d

Cleared Mar 02, 1982

CUTTERBOND ZINC PHOSPHATE CEMENT

Physical Medicine · 13d

TOTAL PARENTERAL NUTRITION SET BAG

K801652 · KPE

General Hospital · 40d

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Cutter Laboratories, Inc. - FDA 510(k) Cleared Devices

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