FDA 510(k)

NCTC 109 MEDIUM

K-Number: K861871 · 1986-05-29

ApplicantHazleton Research Products, Inc.

Decision Date1986-05-29

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

NCTC 109 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 1986-05-29 under 510(k) number K861871. 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 NCTC 109 MEDIUM?

NCTC 109 MEDIUM is a medical device that received FDA 510(k) clearance on 1986-05-29. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K861871.

When did NCTC 109 MEDIUM receive FDA 510(k) clearance?

NCTC 109 MEDIUM received FDA 510(k) clearance on 1986-05-29, under 510(k) number K861871.

Who is the listed applicant for NCTC 109 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 NCTC 109 MEDIUM?

The FDA product code for NCTC 109 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.