LIFE LITE EMERGENCY STRETCHER— 510(k) K920805

Name: FDA 510(k) clearance K920805
Creator: U.S. Food and Drug Administration
Published: 1992-05-22

Substantially Equivalent

Design Principles, Inc.

FDA 510(k) clearance K920805 for LIFE LITE EMERGENCY STRETCHER, Substantially Equivalent on 1992-05-22. Applicant: Design Principles, Inc.. Device class: 1.

Clearance details

Applicant: Design Principles, Inc.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1992-02-21
Decision date: 1992-05-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, AL, US

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