Medical Device Manufacturer · US , Temecula , CA

Granbio, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1987

Recent clearances: EBNA ENZYME IMMUNOASSAY KIT, UNKNOWN, EIA FOR IGG ANTIBODY TO EBV VCA IN HUMAN SERUM

View 8 510(k) Devices ↓

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Cleared

Denied

Granbio, Inc. has 8 FDA 510(k) cleared medical devices. Based in Temecula, US.

Historical record: 8 cleared submissions from 1987 to 1996. Primary specialty: Microbiology.

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

Granbio, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Granbio, Inc.

8 devices

1-8 of 8

Cleared Feb 15, 1996

EBNA ENZYME IMMUNOASSAY KIT

EIA FOR IGG ANTIBODY TO EBV VCA IN HUMAN SERUM

K901156 · GNP

Microbiology · 183d

Cleared Sep 12, 1990

(EIA) FOR IGM ANTIBODY TO EBV VCA IN HUMAN SERUM

K901840 · LJN

Microbiology · 141d

Cleared Jun 07, 1988

INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY

INDIRECT IMMUNOFLUORESCENT ANTIBODY ASSAY/ EBV-VCA

K864347 · GNP

Microbiology · 90d

Cleared Feb 02, 1987

EBV VCA IGM ANTIBODY ASSAY KIT

K864604 · LJN

Microbiology · 70d

Granbio, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Granbio, Inc.

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