PENICILLIN/STREPTOMYCIN SOLUTION— 510(k) K854567

Name: FDA 510(k) clearance K854567
Creator: U.S. Food and Drug Administration
Published: 1985-12-06

Substantially Equivalent

Mediatech, Inc.

FDA 510(k) clearance K854567 for PENICILLIN/STREPTOMYCIN SOLUTION, Substantially Equivalent on 1985-12-06. 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: 1985-11-14
Decision date: 1985-12-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herndon, VA, US

Download summary PDF View on FDA.gov ↗

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

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