MODEL 500 PEDIATRIC STRETCHER/CRIB— 510(k) K852422

Name: FDA 510(k) clearance K852422
Creator: U.S. Food and Drug Administration
Published: 1985-07-05

Substantially Equivalent

Midmark Corp.

FDA 510(k) clearance K852422 for MODEL 500 PEDIATRIC STRETCHER/CRIB, Substantially Equivalent on 1985-07-05. Applicant: Midmark Corp.. Device class: 2.

Clearance details

Applicant: Midmark Corp.
Product code: Code FMS
Device class: Class 2
Regulation: 21 CFR 880.5140
Advisory panel: General Hospital
Date received: 1985-06-07
Decision date: 1985-07-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Versailles, OH, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.