WEEVAC TC HAND CARRIED RESCUE STRETCHER— 510(k) K910709

Name: FDA 510(k) clearance K910709
Creator: U.S. Food and Drug Administration
Published: 1991-04-01

Substantially Equivalent

W. Murphy Ent., Inc.

FDA 510(k) clearance K910709 for WEEVAC TC HAND CARRIED RESCUE STRETCHER, Substantially Equivalent on 1991-04-01. Applicant: W. Murphy Ent., Inc.. Device class: 1.

Clearance details

Applicant: W. Murphy Ent., Inc.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1991-02-20
Decision date: 1991-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ontario, CA

Download summary PDF View on FDA.gov ↗

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