Medical Device Manufacturer · US , UT

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

57 submissions · 57 cleared · Since 1977

Total

Cleared

Denied

Gull Laboratories, Inc. has 57 FDA 510(k) cleared microbiology devices. Based in US.

Historical record: 57 cleared submissions from 1977 to 1999.

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

Gull Laboratories, 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 - Gull Laboratories, Inc.

57 devices

1-12 of 57

Cleared Feb 26, 1999

HSV 1+2 IGG ELISA TEST

K983541 · LGC

Microbiology · 140d

Cleared Nov 04, 1997

MUMPS IGG ELISA TESTY

EBV-EA(D) IGG ELISA TEST

PROTECTORAL ULTRASONIC HANDPIECE PROCESSOR

K932333 · EFB

Dental · 824d

Cleared Aug 04, 1995

RUBELLA IGG ELISA TEST

K941624 · LFX

Microbiology · 487d

Cleared Oct 05, 1992

HSV-1 IGM ELISA TEST -- MODIFICATION

K922758 · LGC

Microbiology · 119d

Cleared Oct 05, 1992

HSV-2 IGM ELISA TEST--MODIFICATION

K922759 · LGC

Microbiology · 119d

Cleared May 04, 1992

CHAGAS' IGG ELISA TEST

K911233 · MIU

Microbiology · 411d

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

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

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