CELLGRO(ISCOVE'S MEDIUM) MODIFICATION— 510(k) K852485

Name: FDA 510(k) clearance K852485
Creator: U.S. Food and Drug Administration
Published: 1985-07-12

Substantially Equivalent

Mediatech, Inc.

FDA 510(k) clearance K852485 for CELLGRO(ISCOVE'S MEDIUM) MODIFICATION, Substantially Equivalent on 1985-07-12. Applicant: Mediatech, Inc.. Device class: 1.

Clearance details

Applicant: Mediatech, Inc.
Product code: Code KIT
Device class: Class 1
Regulation: 21 CFR 864.2220
Advisory panel: Hematology
Date received: 1985-06-11
Decision date: 1985-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

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K852602 — MCCOY'S 5A MEDIUM-LIQUID FORM1985-07-12
K852603 — MCCOY'S 5A MEDIUM - POWDERED FORM1985-07-12

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