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FDA 510(k)

EMB AGAR

K-Number: K821419 · 1982-06-01

ApplicantInterstate Media
Decision Date1982-06-01
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EMB AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Interstate Media. It received FDA 510(k) clearance on 1982-06-01 under 510(k) number K821419. 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 EMB AGAR?

EMB AGAR is a medical device that received FDA 510(k) clearance on 1982-06-01. The listed applicant is Interstate Media. The 510(k) number is K821419.

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

EMB AGAR received FDA 510(k) clearance on 1982-06-01, under 510(k) number K821419.

Who is the listed applicant for EMB AGAR?

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

What is the FDA product code for EMB AGAR?

The FDA product code for EMB AGAR is JSI.

Other records listing Interstate Media 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.

K821425COLUMBIA BLOOD AGAR W/5% SHEEP BLOODK821418TRYPTOSE BLOOD AGAR W/5% SHEEP BLOODK821426STAPHYLOCOCCUS MEDIUM 1100K821420EMB AGARK821430MUELLER HINTON MEDIUMK821422SS AGAR

View all 15 devices →

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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