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FDA 510(k)

TERGITOL 7 AGAR WITH TTC

K-Number: K821775 · 1982-07-02

ApplicantGranite Diagnostics, Inc.
Decision Date1982-07-02
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TERGITOL 7 AGAR WITH TTC 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 1982-07-02 under 510(k) number K821775. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERGITOL 7 AGAR WITH TTC?

TERGITOL 7 AGAR WITH TTC is a medical device that received FDA 510(k) clearance on 1982-07-02. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K821775.

When did TERGITOL 7 AGAR WITH TTC receive FDA 510(k) clearance?

TERGITOL 7 AGAR WITH TTC received FDA 510(k) clearance on 1982-07-02, under 510(k) number K821775.

Who is the listed applicant for TERGITOL 7 AGAR WITH TTC?

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 TERGITOL 7 AGAR WITH TTC?

The FDA product code for TERGITOL 7 AGAR WITH TTC is JSI.

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Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia Manufacturers, Inc.

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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