FDA 510(k)

ALPHA MEM MEDIUM W/O NUCLEOSIDES

K-Number: K850231 · 1985-03-05

ApplicantHazleton Research Products, Inc.

Decision Date1985-03-05

Product Code

DecisionSubstantially Equivalent

Device Summary

ALPHA MEM MEDIUM W/O NUCLEOSIDES 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 1985-03-05 under 510(k) number K850231. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALPHA MEM MEDIUM W/O NUCLEOSIDES?

ALPHA MEM MEDIUM W/O NUCLEOSIDES is a medical device that received FDA 510(k) clearance on 1985-03-05. The listed applicant is Hazleton Research Products, Inc.. The 510(k) number is K850231.

When did ALPHA MEM MEDIUM W/O NUCLEOSIDES receive FDA 510(k) clearance?

ALPHA MEM MEDIUM W/O NUCLEOSIDES received FDA 510(k) clearance on 1985-03-05, under 510(k) number K850231.

Who is the listed applicant for ALPHA MEM MEDIUM W/O NUCLEOSIDES?

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

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.