Medical Device Manufacturer · US , Mchenry , IL

Harvard Apparatus, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1978

Total

Cleared

Denied

Harvard Apparatus, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1978 to 1998. Primary specialty: General Hospital.

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

Harvard Apparatus, Inc. 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 - Harvard Apparatus, Inc.

9 devices

1-9 of 9

Cleared Jan 09, 1998

THE HARVARD LIBRARY

K970678 · MRZ

General Hospital · 319d

Cleared Sep 15, 1995

HARVARD 2 SYRINGE PUMP

K952794 · FRN

General Hospital · 88d

Cleared Dec 14, 1990

HARVARD/LTE LABORATORY STEAM STERILIZER AUTOCLAVE

K903614 · FLE

General Hospital · 127d

Cleared Nov 07, 1990

HARVARD/LTE BENCHTOP STEAM STERILIZER (AUTOCLAVE)

K903613 · FLE

General Hospital · 90d

Cleared Feb 18, 1982

MODEL 2650 HIGH CAPACITY DUAL SYRINGE

K813644 · FRN

General Hospital · 49d

Cleared Aug 27, 1980

SYRINGE INFUSION PUMP #2716

K801904 · FRN

General Hospital · 16d

Cleared Apr 08, 1980

SYRINGE INFUSION PUMP #2720

K800569 · FRN

General Hospital · 25d

Cleared Nov 13, 1979

BATTERY POWERED SYRINGE INFUSION PUMP

K791293 · FRN

General Hospital · 126d

Cleared May 19, 1978

INFUSION PUMP-MODEL 2616

K780705 · FRN

General Hospital · 24d

Harvard Apparatus, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Harvard Apparatus, Inc.

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