MARTIN LEWIS AGAR— 510(k) K850722

Name: FDA 510(k) clearance K850722
Creator: U.S. Food and Drug Administration
Published: 1985-03-22

Substantially Equivalent

Rapid City Regional Hospital, Inc.

FDA 510(k) clearance K850722 for MARTIN LEWIS AGAR, Substantially Equivalent on 1985-03-22. Applicant: Rapid City Regional Hospital, Inc.. Device class: 2.

Clearance details

Applicant: Rapid City Regional Hospital, Inc.
Product code: Code JTY
Device class: Class 2
Regulation: 21 CFR 866.2410
Advisory panel: Microbiology
Date received: 1985-02-22
Decision date: 1985-03-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rapid City, SD, US

Download summary PDF View on FDA.gov ↗

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