EXTRACT BROTH
K-Number: K832570 · 1983-09-12
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Device Summary
Frequently Asked Questions
What is the EXTRACT BROTH?
EXTRACT BROTH is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K832570.
When did EXTRACT BROTH receive FDA 510(k) clearance?
EXTRACT BROTH received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832570.
Who is the listed applicant for EXTRACT 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 EXTRACT BROTH?
The FDA product code for EXTRACT BROTH is JSC.
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: JSC)
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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