MYCAREL AGAR MYCOBROTIC AGAR
K-Number: K823308 · 1982-12-03
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Device Summary
Frequently Asked Questions
What is the MYCAREL AGAR MYCOBROTIC AGAR?
MYCAREL AGAR MYCOBROTIC AGAR is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K823308.
When did MYCAREL AGAR MYCOBROTIC AGAR receive FDA 510(k) clearance?
MYCAREL AGAR MYCOBROTIC AGAR received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823308.
Who is the listed applicant for MYCAREL AGAR MYCOBROTIC AGAR?
The FDA 510(k) record lists Troy Biologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MYCAREL AGAR MYCOBROTIC AGAR?
The FDA product code for MYCAREL AGAR MYCOBROTIC AGAR is JSJ.
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 Troy Biologicals, 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: JSJ)
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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