SYNTEC TRUE LIGHT ENDOILLUMIINATOR WITH PICK— 510(k) K973290

Name: FDA 510(k) clearance K973290
Creator: U.S. Food and Drug Administration
Published: 1997-11-14

Substantially Equivalent

Vaughan Weeks

FDA 510(k) clearance K973290 for SYNTEC TRUE LIGHT ENDOILLUMIINATOR WITH PICK, Substantially Equivalent on 1997-11-14. Applicant: Vaughan Weeks. Device class: 2.

Clearance details

Applicant: Vaughan Weeks
Product code: Code MPA
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1997-09-02
Decision date: 1997-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Caledonia, WI, US

Download summary PDF View on FDA.gov ↗

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