ENDOSCOPIC BLUNT DISSECTING INSTRUMENT— 510(k) K931854

Name: FDA 510(k) clearance K931854
Creator: U.S. Food and Drug Administration
Published: 1993-08-10

Substantially Equivalent

Mayaguez Medical Center

FDA 510(k) clearance K931854 for ENDOSCOPIC BLUNT DISSECTING INSTRUMENT, Substantially Equivalent on 1993-08-10. Applicant: Mayaguez Medical Center. Device class: 2.

Clearance details

Applicant: Mayaguez Medical Center
Product code: Code FGS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1993-04-13
Decision date: 1993-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Trophy Club, TX, US

Download summary PDF View on FDA.gov ↗

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