RESTRAINING STRETCHER— 510(k) K924275

Substantially Equivalent

Dms

FDA 510(k) clearance K924275 for RESTRAINING STRETCHER, Substantially Equivalent on 1993-07-27. Applicant: Dms. Device class: 1.

Clearance details

Applicant: Dms
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1992-08-25
Decision date: 1993-07-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Soiux Falls, SD, US

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