FDA 510(k)

GOAT ANTI-INFLUENZA ANTISERA

K-Number: K780006 · 1978-01-20

ApplicantNortheast Biomedical Labs., Inc.

Decision Date1978-01-20

Product CodeGNS

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

GOAT ANTI-INFLUENZA ANTISERA is the device name listed in this FDA 510(k) record. The listed applicant is Northeast Biomedical Labs., Inc.. It received FDA 510(k) clearance on 1978-01-20 under 510(k) number K780006. The device is classified under product code GNS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOAT ANTI-INFLUENZA ANTISERA?

GOAT ANTI-INFLUENZA ANTISERA is a medical device that received FDA 510(k) clearance on 1978-01-20. The listed applicant is Northeast Biomedical Labs., Inc.. The 510(k) number is K780006.

When did GOAT ANTI-INFLUENZA ANTISERA receive FDA 510(k) clearance?

GOAT ANTI-INFLUENZA ANTISERA received FDA 510(k) clearance on 1978-01-20, under 510(k) number K780006.

Who is the listed applicant for GOAT ANTI-INFLUENZA ANTISERA?

The FDA 510(k) record lists Northeast Biomedical Labs., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GOAT ANTI-INFLUENZA ANTISERA?

The FDA product code for GOAT ANTI-INFLUENZA ANTISERA is GNS.

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Other records listing Northeast Biomedical Labs., Inc. as applicant

K780697GOAT ANTI-INFLUENZA ANTISERA ATEXAS K780696GOAT ANTIINFLUENZA ANTISERA AUSSR K780008GOAT ANTI-INFLUENZA ANTISERA K780004GOAT ANTI-INFLUENZA ANTISERA K780007GOAT ANTI-INFLUENZA ANTISERA K780009GUINEA PIG WHOLE SERUM

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Related Devices (Code: GNS)

K780697GOAT ANTI-INFLUENZA ANTISERA ATEXASNortheast Biomedical Labs., Inc.K780696GOAT ANTIINFLUENZA ANTISERA AUSSRNortheast Biomedical Labs., Inc.K780273INFLUENZA HI PRESERUMFlow Laboratories, Inc.K780274INFLUENZA HI ANTISERUMFlow Laboratories, Inc.K780277INFLUENZA HI PRESERUM A/TEXASFlow Laboratories, Inc.K780276INFLUENZA HI ANTISERUM A/TEXASFlow Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.