M-GREEN YEAST & MOLD BROTH
K-Number: K811336 · 1981-05-29
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Device Summary
Frequently Asked Questions
What is the M-GREEN YEAST & MOLD BROTH?
M-GREEN YEAST & MOLD BROTH is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811336.
When did M-GREEN YEAST & MOLD BROTH receive FDA 510(k) clearance?
M-GREEN YEAST & MOLD BROTH received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811336.
Who is the listed applicant for M-GREEN YEAST & MOLD BROTH?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for M-GREEN YEAST & MOLD BROTH?
The FDA product code for M-GREEN YEAST & MOLD BROTH 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 Acumedia Manufacturers, 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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