MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS— 510(k) K042659

Name: FDA 510(k) clearance K042659
Creator: U.S. Food and Drug Administration
Published: 2005-02-14

Substantially Equivalent

Medisiss

FDA 510(k) clearance K042659 for MEDISISS REPROCESSED NON-ELECTRIC GI BIOPSY FORCEPS, Substantially Equivalent on 2005-02-14. Applicant: Medisiss. Device class: 1.

Clearance details

Applicant: Medisiss
Product code: Code NON
Device class: Class 1
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 2004-09-28
Decision date: 2005-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, OR, US

Download summary PDF View on FDA.gov ↗

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