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FDA 510(k)

CLOSTRIDIUM DIFFICILE AGAR DEEP &

K-Number: K840889 · 1984-03-23

ApplicantRemel Co.
Decision Date1984-03-23
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CLOSTRIDIUM DIFFICILE AGAR DEEP & is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1984-03-23 under 510(k) number K840889. 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 CLOSTRIDIUM DIFFICILE AGAR DEEP &?

CLOSTRIDIUM DIFFICILE AGAR DEEP & is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Remel Co.. The 510(k) number is K840889.

When did CLOSTRIDIUM DIFFICILE AGAR DEEP & receive FDA 510(k) clearance?

CLOSTRIDIUM DIFFICILE AGAR DEEP & received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840889.

Who is the listed applicant for CLOSTRIDIUM DIFFICILE AGAR DEEP &?

The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLOSTRIDIUM DIFFICILE AGAR DEEP &?

The FDA product code for CLOSTRIDIUM DIFFICILE AGAR DEEP & is JSI.

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Other records listing Remel Co. 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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

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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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