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FDA 510(k)

ADENOVIRUS GROUP-FA LABELLED PRESERUM

K-Number: K770811 · 1977-05-20

Decision Date1977-05-20
Product CodeGNY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ADENOVIRUS GROUP-FA LABELLED PRESERUM is the device name listed in this FDA 510(k) record. The listed applicant is Flow Laboratories, Inc.. It received FDA 510(k) clearance on 1977-05-20 under 510(k) number K770811. The device is classified under product code GNY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADENOVIRUS GROUP-FA LABELLED PRESERUM?

ADENOVIRUS GROUP-FA LABELLED PRESERUM is a medical device that received FDA 510(k) clearance on 1977-05-20. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K770811.

When did ADENOVIRUS GROUP-FA LABELLED PRESERUM receive FDA 510(k) clearance?

ADENOVIRUS GROUP-FA LABELLED PRESERUM received FDA 510(k) clearance on 1977-05-20, under 510(k) number K770811.

Who is the listed applicant for ADENOVIRUS GROUP-FA LABELLED PRESERUM?

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

What is the FDA product code for ADENOVIRUS GROUP-FA LABELLED PRESERUM?

The FDA product code for ADENOVIRUS GROUP-FA LABELLED PRESERUM is GNY.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Flow Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 57 devices →

Related Devices (Code: GNY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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