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FDA 510(k)

ACTINOMYCETE DIFFERENTIAL MEDIA

K-Number: K873270 · 1987-11-04

ApplicantCentral Media
Decision Date1987-11-04
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ACTINOMYCETE DIFFERENTIAL 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 1987-11-04 under 510(k) number K873270. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACTINOMYCETE DIFFERENTIAL MEDIA?

ACTINOMYCETE DIFFERENTIAL MEDIA is a medical device that received FDA 510(k) clearance on 1987-11-04. The listed applicant is Central Media. The 510(k) number is K873270.

When did ACTINOMYCETE DIFFERENTIAL MEDIA receive FDA 510(k) clearance?

ACTINOMYCETE DIFFERENTIAL MEDIA received FDA 510(k) clearance on 1987-11-04, under 510(k) number K873270.

Who is the listed applicant for ACTINOMYCETE DIFFERENTIAL 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 ACTINOMYCETE DIFFERENTIAL MEDIA?

The FDA product code for ACTINOMYCETE DIFFERENTIAL MEDIA is JSH.

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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.

K873259SPECIALTY MEDIAK873258STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIAK873257GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.K873260CORYNEBACTERIA ISOLATION MEDIAK873267ECG BASED MEDIAK873268MUELLER HINTON MEDIA

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Related Devices (Code: JSH)

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.

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia 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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