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FDA 510(k)

CELLGRO WILLIAMS' MEDIUM E

K-Number: K852475 · 1985-07-12

ApplicantMediatech, Inc.
Decision Date1985-07-12
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CELLGRO WILLIAMS' MEDIUM E is the device name listed in this FDA 510(k) record. The listed applicant is Mediatech, Inc.. It received FDA 510(k) clearance on 1985-07-12 under 510(k) number K852475. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CELLGRO WILLIAMS' MEDIUM E?

CELLGRO WILLIAMS' MEDIUM E is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is Mediatech, Inc.. The 510(k) number is K852475.

When did CELLGRO WILLIAMS' MEDIUM E receive FDA 510(k) clearance?

CELLGRO WILLIAMS' MEDIUM E received FDA 510(k) clearance on 1985-07-12, under 510(k) number K852475.

Who is the listed applicant for CELLGRO WILLIAMS' MEDIUM E?

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

What is the FDA product code for CELLGRO WILLIAMS' MEDIUM E?

The FDA product code for CELLGRO WILLIAMS' MEDIUM E is KIT.

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Other records listing Mediatech, Inc. as applicant

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K860623CELLGRO HEPES BUFFER SOLUTIONK854567PENICILLIN/STREPTOMYCIN SOLUTIONK852485CELLGRO(ISCOVE'S MEDIUM) MODIFICATIONK852602MCCOY'S 5A MEDIUM-LIQUID FORMK852603MCCOY'S 5A MEDIUM - POWDERED FORMK852288CELLGRO

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Related Devices (Code: KIT)

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.

K892938AMNIO-GROW TMInovar Biologicals, Inc.K890700MELANOCYTE GROWTH MEDIUM (MGM)Clonetics Corp.K890701ENDOTHELIAL GROWTH MEDIUM (EGM)Clonetics Corp.K890482ABC, ABC-1X, ABC(TM)Cell Ent., Inc.K884654ALPHACALF SERUMHyclone Laboratories, Inc.K884572RPMI-1640 HYBRI-MAX, PROD. NO. R5382Sigma Chemical Co.

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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