MEMCATH UROLOGY INTRODUCER SHEATH, MODEL 201— 510(k) K000767

Name: FDA 510(k) clearance K000767
Creator: U.S. Food and Drug Administration
Published: 2000-06-05

Substantially Equivalent

Memcath Technologies, LLC

FDA 510(k) clearance K000767 for MEMCATH UROLOGY INTRODUCER SHEATH, MODEL 201, Substantially Equivalent on 2000-06-05. Applicant: Memcath Technologies, LLC. Device class: 2.

Clearance details

Applicant: Memcath Technologies, LLC
Product code: Code KNY
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 2000-03-09
Decision date: 2000-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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