SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES— 510(k) K030919

Name: FDA 510(k) clearance K030919
Creator: U.S. Food and Drug Administration
Published: 2003-07-03

Substantially Equivalent

Medisiss

FDA 510(k) clearance K030919 for SISS, INC. (D.B.A.MEDISISS) REPROCESSD ELECTROSURGICAL INSTRUMENTS AND ACCESSORIES, Substantially Equivalent on 2003-07-03. Applicant: Medisiss. Device class: 2.

Clearance details

Applicant: Medisiss
Product code: Code NLR
Device class: Class 2
Regulation: 21 CFR 876.4300
Advisory panel: Gastroenterology, Urology
Date received: 2003-03-24
Decision date: 2003-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sisters, OR, US

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