ADENOVIRUS GROUP-FA LABELLED PRESERUM
K-Number: K770811 · 1977-05-20
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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