329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR— 510(k) K852253

Name: FDA 510(k) clearance K852253
Creator: U.S. Food and Drug Administration
Published: 1985-07-29

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K852253 for 329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR, Substantially Equivalent on 1985-07-29. Applicant: Cordis Corp.. Device class: 2.

Clearance details

Applicant: Cordis Corp.
Product code: Code DTD
Device class: Class 2
Regulation: 21 CFR 870.3620
Advisory panel: Cardiovascular
Date received: 1985-05-24
Decision date: 1985-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

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