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FDA 510(k)

CORYNEBACTERIA ISOLATION MEDIA

K-Number: K873260 · 1987-11-06

ApplicantCentral Media
Decision Date1987-11-06
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CORYNEBACTERIA ISOLATION MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Central Media. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873260. 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 CORYNEBACTERIA ISOLATION MEDIA?

CORYNEBACTERIA ISOLATION MEDIA is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Central Media. The 510(k) number is K873260.

When did CORYNEBACTERIA ISOLATION MEDIA receive FDA 510(k) clearance?

CORYNEBACTERIA ISOLATION MEDIA received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873260.

Who is the listed applicant for CORYNEBACTERIA ISOLATION MEDIA?

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

What is the FDA product code for CORYNEBACTERIA ISOLATION MEDIA?

The FDA product code for CORYNEBACTERIA ISOLATION MEDIA is JSI.

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Other records listing Central 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.

K873257GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.K873259SPECIALTY MEDIAK873258STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIAK873267ECG BASED MEDIAK873270ACTINOMYCETE DIFFERENTIAL MEDIAK873268MUELLER HINTON MEDIA

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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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