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FDA 510(k)

VOGEL & JOHNSON AGAR

K-Number: K811039 · 1981-05-05

ApplicantAcumedia Manufacturers, Inc.
Decision Date1981-05-05
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VOGEL & JOHNSON AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1981-05-05 under 510(k) number K811039. 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 VOGEL & JOHNSON AGAR?

VOGEL & JOHNSON AGAR is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811039.

When did VOGEL & JOHNSON AGAR receive FDA 510(k) clearance?

VOGEL & JOHNSON AGAR received FDA 510(k) clearance on 1981-05-05, under 510(k) number K811039.

Who is the listed applicant for VOGEL & JOHNSON AGAR?

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

What is the FDA product code for VOGEL & JOHNSON AGAR?

The FDA product code for VOGEL & JOHNSON AGAR is JSI.

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Other records listing Acumedia Manufacturers, Inc. 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.

K881534ANTIBIOTIC MEDIUM #9 POLYMYXIN BASE AGARK881540FLO AGARK881544LITTMAN AGARK881561TERGITOL 7 BROTHK881575SELECTIVE STREPTOCOCCUS AGARK881569STUARTS TRANSPORT MEDIUM

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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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