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FDA 510(k)

BIGGY AGAR

K-Number: K830082 · 1983-02-10

ApplicantbioMerieux, Inc.
Decision Date1983-02-10
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BIGGY 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 1983-02-10 under 510(k) number K830082. 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 BIGGY AGAR?

BIGGY AGAR is a medical device that received FDA 510(k) clearance on 1983-02-10. The listed applicant is bioMerieux, Inc.. The 510(k) number is K830082.

When did BIGGY AGAR receive FDA 510(k) clearance?

BIGGY AGAR received FDA 510(k) clearance on 1983-02-10, under 510(k) number K830082.

Who is the listed applicant for BIGGY 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 BIGGY AGAR?

The FDA product code for BIGGY AGAR 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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