FDA 510(k)

SELECTIVE AND DIFFERENTIAL

K-Number: K841209 · 1984-04-17

Decision Date1984-04-17

Product CodeJSI

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

SELECTIVE AND DIFFERENTIAL is the device name listed in this FDA 510(k) record. The listed applicant is Smith River Biologicals. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K841209. 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 SELECTIVE AND DIFFERENTIAL?

SELECTIVE AND DIFFERENTIAL is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Smith River Biologicals. The 510(k) number is K841209.

When did SELECTIVE AND DIFFERENTIAL receive FDA 510(k) clearance?

SELECTIVE AND DIFFERENTIAL received FDA 510(k) clearance on 1984-04-17, under 510(k) number K841209.

Who is the listed applicant for SELECTIVE AND DIFFERENTIAL?

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

What is the FDA product code for SELECTIVE AND DIFFERENTIAL?

The FDA product code for SELECTIVE AND DIFFERENTIAL is JSI.

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Other records listing Smith River Biologicals as applicant

K923892SMITH RIVER MICROBIOLOGICAL CULTURE MEDIA K841206NON-SELECTIVE & DIFFERENTIAL K841207NON-SELECTIVE & NON-DIFFERENTIAL K841204MULTIPLE BIOCHEMICAL TEST K841208PROPAGATING TRANSPORT K841211SELECTIVE BROTH

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Related Devices (Code: JSI)

K070691BBL CHROMAGAR 0157Becton, Dickinson & CO K974428DIPSTREAKNovamed , 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.