YEAST ASSIMILATION AGAR
K-Number: K760764 · 1976-10-29
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Device Summary
Frequently Asked Questions
What is the YEAST ASSIMILATION AGAR?
YEAST ASSIMILATION AGAR is a medical device that received FDA 510(k) clearance on 1976-10-29. The listed applicant is Bioquest. The 510(k) number is K760764.
When did YEAST ASSIMILATION AGAR receive FDA 510(k) clearance?
YEAST ASSIMILATION AGAR received FDA 510(k) clearance on 1976-10-29, under 510(k) number K760764.
Who is the listed applicant for YEAST ASSIMILATION AGAR?
The FDA 510(k) record lists Bioquest as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YEAST ASSIMILATION AGAR?
The FDA product code for YEAST ASSIMILATION AGAR is JSG.
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 Bioquest 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: JSG)
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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