MODEL #520/525 ED/RECOVERY STRETCHER— 510(k) K894987

Name: FDA 510(k) clearance K894987
Creator: U.S. Food and Drug Administration
Published: 1989-09-05

Substantially Equivalent

Medmark, Inc.

FDA 510(k) clearance K894987 for MODEL #520/525 ED/RECOVERY STRETCHER, Substantially Equivalent on 1989-09-05. Applicant: Medmark, Inc.. Device class: 1.

Clearance details

Applicant: Medmark, Inc.
Product code: Code INW
Device class: Class 1
Regulation: 21 CFR 890.3750
Advisory panel: Physical Medicine
Date received: 1989-08-08
Decision date: 1989-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Versailles, OH, US

Download summary PDF View on FDA.gov ↗

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