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FDA 510(k)

HAM'S F-12 W/NAHCO3

K-Number: K860785 · 1986-03-12

ApplicantTissue Culture Innovations
Decision Date1986-03-12
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HAM'S F-12 W/NAHCO3 is the device name listed in this FDA 510(k) record. The listed applicant is Tissue Culture Innovations. It received FDA 510(k) clearance on 1986-03-12 under 510(k) number K860785. 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 HAM'S F-12 W/NAHCO3?

HAM'S F-12 W/NAHCO3 is a medical device that received FDA 510(k) clearance on 1986-03-12. The listed applicant is Tissue Culture Innovations. The 510(k) number is K860785.

When did HAM'S F-12 W/NAHCO3 receive FDA 510(k) clearance?

HAM'S F-12 W/NAHCO3 received FDA 510(k) clearance on 1986-03-12, under 510(k) number K860785.

Who is the listed applicant for HAM'S F-12 W/NAHCO3?

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

What is the FDA product code for HAM'S F-12 W/NAHCO3?

The FDA product code for HAM'S F-12 W/NAHCO3 is KIT.

Related Clinical Trials

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.

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Other records listing Tissue Culture Innovations 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.

K860784DULBECCO'S PHOSPHATE BUFFERED SALINE W/CALCL2K860786RPMI 1640 HEPESK860787DULBECCO'S MEMK860783MICRO CARRIERK860788HAM'S F-12 W/GLUTAMINE & NAHCO3

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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