TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER— 510(k) K931201

Name: FDA 510(k) clearance K931201
Creator: U.S. Food and Drug Administration
Published: 1993-09-28

Substantially Equivalent

Tri-Med Specialties, Inc.

FDA 510(k) clearance K931201 for TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETER, Substantially Equivalent on 1993-09-28. Applicant: Tri-Med Specialties, Inc.. Device class: 2.

Clearance details

Applicant: Tri-Med Specialties, Inc.
Product code: Code OCX
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-03-09
Decision date: 1993-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Overland Park, KS, US

Download summary PDF View on FDA.gov ↗

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