FDA 510(k)

RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER

K-Number: K861875 · 1986-05-29

ApplicantHazleton Research Products, Inc.

Decision Date1986-05-29

Product CodeKIT

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER 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 K861875. 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 MEDIUM WITH 25MM HEPES BUFFER?

RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER 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 K861875.

When did RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER receive FDA 510(k) clearance?

RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER received FDA 510(k) clearance on 1986-05-29, under 510(k) number K861875.

Who is the listed applicant for RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER?

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 RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER?

The FDA product code for RPMI-1640 MEDIUM WITH 25MM HEPES BUFFER is KIT.

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Other records listing Hazleton Research Products, Inc. as applicant

K861997PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE K861996DULBECCO'S MEM WITH 4.5 G/L GLUCOSE MEDIUM K861886DMEM & HAM'S F-12 (1:1) POWDERED MEDIUM K861869GENTAMICIN-50MG/ML K861872ISCOVE'S (MODIFIED) DULBECCO'S MEDIUM K861871NCTC 109 MEDIUM

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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.