THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE— 510(k) K121135

Name: FDA 510(k) clearance K121135
Creator: U.S. Food and Drug Administration
Published: 2012-06-01

Substantially Equivalent

Thd Spa

FDA 510(k) clearance K121135 for THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE, Substantially Equivalent on 2012-06-01. Applicant: Thd Spa. Device class: 2.

Clearance details

Applicant: Thd Spa
Product code: Code FER
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2012-04-13
Decision date: 2012-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Imoa, IT

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.