VICKERS MEDICAL MODEL 112 TREONIC DC2— 510(k) K791645

Name: FDA 510(k) clearance K791645
Creator: U.S. Food and Drug Administration
Published: 1979-10-02

Substantially Equivalent

Vickers America Medical Corp.

FDA 510(k) clearance K791645 for VICKERS MEDICAL MODEL 112 TREONIC DC2, Substantially Equivalent on 1979-10-02. Applicant: Vickers America Medical Corp.. Device class: 2.

Clearance details

Applicant: Vickers America Medical Corp.
Product code: Code FKW
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1979-08-23
Decision date: 1979-10-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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