MARTIN-LEWIS MEDIUM— 510(k) K782117

Name: FDA 510(k) clearance K782117
Creator: U.S. Food and Drug Administration
Published: 1979-02-01

Substantially Equivalent

Prepared Media Laboratory, Inc.

FDA 510(k) clearance K782117 for MARTIN-LEWIS MEDIUM, Substantially Equivalent on 1979-02-01. Applicant: Prepared Media Laboratory, Inc.. Device class: 2.

Clearance details

Applicant: Prepared Media Laboratory, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1978-12-27
Decision date: 1979-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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