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FDA 510(k)

MEM GLASGOW POWDERED MEDIUM

K-Number: K861887 · 1986-05-29

ApplicantHazleton Research Products, Inc.
Decision Date1986-05-29
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MEM GLASGOW POWDERED 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 K861887. 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 MEM GLASGOW POWDERED MEDIUM?

MEM GLASGOW POWDERED 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 K861887.

When did MEM GLASGOW POWDERED MEDIUM receive FDA 510(k) clearance?

MEM GLASGOW POWDERED MEDIUM received FDA 510(k) clearance on 1986-05-29, under 510(k) number K861887.

Who is the listed applicant for MEM GLASGOW POWDERED 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 MEM GLASGOW POWDERED MEDIUM?

The FDA product code for MEM GLASGOW POWDERED MEDIUM is KIT.

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Other records listing Hazleton Research Products, Inc. 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.

K861997PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTUREK861996DULBECCO'S MEM WITH 4.5 G/L GLUCOSE MEDIUMK861886DMEM & HAM'S F-12 (1:1) POWDERED MEDIUMK861869GENTAMICIN-50MG/MLK861872ISCOVE'S (MODIFIED) DULBECCO'S MEDIUMK861871NCTC 109 MEDIUM

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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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