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FDA 510(k)

TISSUE CULTURE MEDIA W/HEPES BUFFER

K-Number: K770764 · 1977-07-21

ApplicantMicrobiological Assoc.
Decision Date1977-07-21
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TISSUE CULTURE MEDIA W/HEPES BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Microbiological Assoc.. It received FDA 510(k) clearance on 1977-07-21 under 510(k) number K770764. 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 TISSUE CULTURE MEDIA W/HEPES BUFFER?

TISSUE CULTURE MEDIA W/HEPES BUFFER is a medical device that received FDA 510(k) clearance on 1977-07-21. The listed applicant is Microbiological Assoc.. The 510(k) number is K770764.

When did TISSUE CULTURE MEDIA W/HEPES BUFFER receive FDA 510(k) clearance?

TISSUE CULTURE MEDIA W/HEPES BUFFER received FDA 510(k) clearance on 1977-07-21, under 510(k) number K770764.

Who is the listed applicant for TISSUE CULTURE MEDIA W/HEPES BUFFER?

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

What is the FDA product code for TISSUE CULTURE MEDIA W/HEPES BUFFER?

The FDA product code for TISSUE CULTURE MEDIA W/HEPES BUFFER is KIT.

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Other records listing Microbiological Assoc. 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.

K792133RUBELISA TEST KITK791397HERPES EIA TEST KITK781549TOXELISA TEST KITK780996RUBELISA TEST KITK781392CYTOMEGILISH TEST KITK781143IMMUNOFLUORESCENCE TEST 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

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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