STRYKER ECLIPSE WARMING STRETCHER— 510(k) K912237

Name: FDA 510(k) clearance K912237
Creator: U.S. Food and Drug Administration
Published: 1991-07-30

Substantially Equivalent

Stryker Medical

FDA 510(k) clearance K912237 for STRYKER ECLIPSE WARMING STRETCHER, Substantially Equivalent on 1991-07-30. Applicant: Stryker Medical. Device class: 1.

Clearance details

Applicant: Stryker Medical
Product code: Code DWI
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1991-05-21
Decision date: 1991-07-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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