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FDA 510(k)

SERUM FREE TISSUE CULTURE MEDIA

K-Number: K803041 · 1980-12-30

ApplicantCartaya Assoc.
Decision Date1980-12-30
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SERUM FREE TISSUE CULTURE MEDIA is the device name listed in this FDA 510(k) record. The listed applicant is Cartaya Assoc.. It received FDA 510(k) clearance on 1980-12-30 under 510(k) number K803041. 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 SERUM FREE TISSUE CULTURE MEDIA?

SERUM FREE TISSUE CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Cartaya Assoc.. The 510(k) number is K803041.

When did SERUM FREE TISSUE CULTURE MEDIA receive FDA 510(k) clearance?

SERUM FREE TISSUE CULTURE MEDIA received FDA 510(k) clearance on 1980-12-30, under 510(k) number K803041.

Who is the listed applicant for SERUM FREE TISSUE CULTURE MEDIA?

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

What is the FDA product code for SERUM FREE TISSUE CULTURE MEDIA?

The FDA product code for SERUM FREE TISSUE CULTURE MEDIA is KIT.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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