SKED STRETCHER— 510(k) K896177

Substantially Equivalent

Skedco, Inc.

FDA 510(k) clearance K896177 for SKED STRETCHER, Substantially Equivalent on 1990-01-11. Applicant: Skedco, Inc.. Device class: 1.

Clearance details

Applicant: Skedco, Inc.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1989-10-25
Decision date: 1990-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, 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.