FDA 510(k)

HAM'S MIXTURE F-12 MEDIUM

K-Number: K850227 · 1985-03-11

ApplicantHazleton Research Products, Inc.

Decision Date1985-03-11

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

HAM'S MIXTURE F-12 MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Hazleton Research Products, Inc.. It received FDA 510(k) clearance on 1985-03-11 under 510(k) number K850227. 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 MIXTURE F-12 MEDIUM?

HAM'S MIXTURE F-12 MEDIUM is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850227.

When did HAM'S MIXTURE F-12 MEDIUM receive FDA 510(k) clearance?

HAM'S MIXTURE F-12 MEDIUM received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850227.

Who is the listed applicant for HAM'S MIXTURE F-12 MEDIUM?

The FDA 510(k) record lists Hazleton Research Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAM'S MIXTURE F-12 MEDIUM?

The FDA product code for HAM'S MIXTURE F-12 MEDIUM is KIT.

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Other records listing Hazleton Research Products, Inc. as applicant

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Related Devices (Code: KIT)

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.