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FDA 510(k)

JORDANS TARTRATE AGAR

K-Number: K822996 · 1982-11-16

ApplicantGranite Diagnostics, Inc.
Decision Date1982-11-16
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

JORDANS TARTRATE AGAR 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 1982-11-16 under 510(k) number K822996. 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 JORDANS TARTRATE AGAR?

JORDANS TARTRATE AGAR is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K822996.

When did JORDANS TARTRATE AGAR receive FDA 510(k) clearance?

JORDANS TARTRATE AGAR received FDA 510(k) clearance on 1982-11-16, under 510(k) number K822996.

Who is the listed applicant for JORDANS TARTRATE AGAR?

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 JORDANS TARTRATE AGAR?

The FDA product code for JORDANS TARTRATE AGAR is 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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