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FDA 510(k)

CELL CULTURE REFEED MEDIUM

K-Number: K850537 · 1985-03-20

ApplicantHillcrest Biologicals
Decision Date1985-03-20
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CELL CULTURE REFEED MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Hillcrest Biologicals. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850537. 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 CELL CULTURE REFEED MEDIUM?

CELL CULTURE REFEED MEDIUM is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Hillcrest Biologicals. The 510(k) number is K850537.

When did CELL CULTURE REFEED MEDIUM receive FDA 510(k) clearance?

CELL CULTURE REFEED MEDIUM received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850537.

Who is the listed applicant for CELL CULTURE REFEED MEDIUM?

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

What is the FDA product code for CELL CULTURE REFEED MEDIUM?

The FDA product code for CELL CULTURE REFEED MEDIUM is KIT.

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Other records listing Hillcrest Biologicals 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.

K913617ARBOVIRUS IGG IFA TESTK913618ARBOVIRUS IGM IFA TESTK913906Q FEVER IGG IFA TESTK922374Q FEVER IGM IFA TESTK900206LYME DISEASE IGM ELISAK896594EBV VCA ANTIBODY (IGM)

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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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