STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER— 510(k) K940130

Name: FDA 510(k) clearance K940130
Creator: U.S. Food and Drug Administration
Published: 1994-03-10

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K940130 for STRYKER MODEL 6110 EMERGENCY/POLE STRETCHER, Substantially Equivalent on 1994-03-10. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code FPP
Device class: Class 1
Regulation: 21 CFR 880.6900
Advisory panel: General Hospital
Date received: 1994-01-03
Decision date: 1994-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, 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.