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FDA 510(k)

RPMI 1640 HEPES

K-Number: K860786 · 1986-03-12

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

Device Summary

RPMI 1640 HEPES 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 K860786. 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 RPMI 1640 HEPES?

RPMI 1640 HEPES 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 K860786.

When did RPMI 1640 HEPES receive FDA 510(k) clearance?

RPMI 1640 HEPES received FDA 510(k) clearance on 1986-03-12, under 510(k) number K860786.

Who is the listed applicant for RPMI 1640 HEPES?

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 RPMI 1640 HEPES?

The FDA product code for RPMI 1640 HEPES is KIT.

Related Clinical Trials

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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.

K860785HAM'S F-12 W/NAHCO3K860784DULBECCO'S PHOSPHATE BUFFERED SALINE W/CALCL2K860787DULBECCO'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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