DAYTRIPPER DIALYSATE WARMER— 510(k) K020542

Name: FDA 510(k) clearance K020542
Creator: U.S. Food and Drug Administration
Published: 2002-09-27

Substantially Equivalent

Stickman Industries, Inc.

FDA 510(k) clearance K020542 for DAYTRIPPER DIALYSATE WARMER, Substantially Equivalent on 2002-09-27. Applicant: Stickman Industries, Inc.. Device class: 2.

Clearance details

Applicant: Stickman Industries, Inc.
Product code: Code MLW
Device class: Class 2
Regulation: 21 CFR 876.5630
Advisory panel: Gastroenterology, Urology
Date received: 2002-02-19
Decision date: 2002-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ottawa, Ontario, CA

Download summary PDF View on FDA.gov ↗

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