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FDA 510(k)

V AGAR

K-Number: K832954 · 1983-09-29

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1983-09-29
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

V AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832954. 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 V AGAR?

V AGAR is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K832954.

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

V AGAR received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832954.

Who is the listed applicant for V AGAR?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V AGAR?

The FDA product code for V 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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