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FDA 510(k)

YEAST ASSIMILATION BROTH

K-Number: K822694 · 1982-09-30

ApplicantGranite Diagnostics, Inc.
Decision Date1982-09-30
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YEAST ASSIMILATION BROTH is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822694. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YEAST ASSIMILATION BROTH?

YEAST ASSIMILATION BROTH is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K822694.

When did YEAST ASSIMILATION BROTH receive FDA 510(k) clearance?

YEAST ASSIMILATION BROTH received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822694.

Who is the listed applicant for YEAST ASSIMILATION BROTH?

The FDA 510(k) record lists Granite Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YEAST ASSIMILATION BROTH?

The FDA product code for YEAST ASSIMILATION BROTH is JSF.

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Other records listing Granite Diagnostics, Inc. as applicant

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Related Devices (Code: JSF)

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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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