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FDA 510(k)

YERSINIA SELECTIVE AGAR

K-Number: K844535 · 1985-01-05

ApplicantbioMerieux, Inc.
Decision Date1985-01-05
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YERSINIA SELECTIVE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1985-01-05 under 510(k) number K844535. 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 YERSINIA SELECTIVE AGAR?

YERSINIA SELECTIVE AGAR is a medical device that received FDA 510(k) clearance on 1985-01-05. The listed applicant is bioMerieux, Inc.. The 510(k) number is K844535.

When did YERSINIA SELECTIVE AGAR receive FDA 510(k) clearance?

YERSINIA SELECTIVE AGAR received FDA 510(k) clearance on 1985-01-05, under 510(k) number K844535.

Who is the listed applicant for YERSINIA SELECTIVE AGAR?

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

What is the FDA product code for YERSINIA SELECTIVE AGAR?

The FDA product code for YERSINIA SELECTIVE AGAR is JSI.

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Related Devices (Code: JSI)

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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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