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FDA 510(k)

ROGOSA BROTH

K-Number: K832310 · 1983-09-01

Decision Date1983-09-01
Product CodeJSD
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ROGOSA BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1983-09-01 under 510(k) number K832310. The device is classified under product code JSD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROGOSA BROTH?

ROGOSA BROTH is a medical device that received FDA 510(k) clearance on 1983-09-01. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K832310.

When did ROGOSA BROTH receive FDA 510(k) clearance?

ROGOSA BROTH received FDA 510(k) clearance on 1983-09-01, under 510(k) number K832310.

Who is the listed applicant for ROGOSA BROTH?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ROGOSA BROTH?

The FDA product code for ROGOSA BROTH is JSD.

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 Oxoid U.S.A., 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: JSD)

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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