VISITEC NEEDLE RANGE (GASTERUROLOGY)— 510(k) K811965

Name: FDA 510(k) clearance K811965
Creator: U.S. Food and Drug Administration
Published: 1981-08-25

Substantially Equivalent

Visitec Co.

FDA 510(k) clearance K811965 for VISITEC NEEDLE RANGE (GASTERUROLOGY), Substantially Equivalent on 1981-08-25. Applicant: Visitec Co.. Device class: 1.

Clearance details

Applicant: Visitec Co.
Product code: Code FHR
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1981-07-10
Decision date: 1981-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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