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FDA 510(k)

BILE ESCULIN MEDIA

K-Number: K811600 · 1981-06-25

ApplicantMicro Media Laboratories
Decision Date1981-06-25
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BILE ESCULIN MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1981-06-25 under 510(k) number K811600. 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 BILE ESCULIN MEDIA?

BILE ESCULIN MEDIA is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Micro Media Laboratories. The 510(k) number is K811600.

When did BILE ESCULIN MEDIA receive FDA 510(k) clearance?

BILE ESCULIN MEDIA received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811600.

Who is the listed applicant for BILE ESCULIN MEDIA?

The FDA 510(k) record lists Micro Media Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BILE ESCULIN MEDIA?

The FDA product code for BILE ESCULIN MEDIA is JSI.

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Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851343BROM CRESOL PURPLE STARCHK851348COBA AGAR

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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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