ARM AUTOMATIC REPROCESSING MACHINE— 510(k) K013713

Name: FDA 510(k) clearance K013713
Creator: U.S. Food and Drug Administration
Published: 2002-07-15

Substantially Equivalent

Alcavis International Incorporated

FDA 510(k) clearance K013713 for ARM AUTOMATIC REPROCESSING MACHINE, Substantially Equivalent on 2002-07-15. Applicant: Alcavis International Incorporated. Device class: 2.

Clearance details

Applicant: Alcavis International Incorporated
Product code: Code LIF
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 2001-11-08
Decision date: 2002-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gaithersburg, MD, US

Download summary PDF View on FDA.gov ↗

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