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FDA 510(k)

ANTIBIOTIC ASSAY BROTH

K-Number: K832575 · 1983-09-12

Decision Date1983-09-12
Product CodeJSA
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ANTIBIOTIC ASSAY BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832575. The device is classified under product code JSA. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTIBIOTIC ASSAY BROTH?

ANTIBIOTIC ASSAY 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 K832575.

When did ANTIBIOTIC ASSAY BROTH receive FDA 510(k) clearance?

ANTIBIOTIC ASSAY BROTH received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832575.

Who is the listed applicant for ANTIBIOTIC ASSAY 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 ANTIBIOTIC ASSAY BROTH?

The FDA product code for ANTIBIOTIC ASSAY BROTH is JSA.

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.

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Related Devices (Code: JSA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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