MEHTA BRONCHIAL BIOSPY DRILL— 510(k) K954693

Name: FDA 510(k) clearance K954693
Creator: U.S. Food and Drug Administration
Published: 1995-10-23

Substantially Equivalent

United States Endoscopy Group, Inc.

FDA 510(k) clearance K954693 for MEHTA BRONCHIAL BIOSPY DRILL, Substantially Equivalent on 1995-10-23. Applicant: United States Endoscopy Group, Inc.. Device class: 2.

Clearance details

Applicant: United States Endoscopy Group, Inc.
Product code: Code FCK
Device class: Class 2
Regulation: 21 CFR 876.1075
Advisory panel: Gastroenterology, Urology
Date received: 1995-10-11
Decision date: 1995-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mentor, OH, US

Download summary PDF View on FDA.gov ↗

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