PACEART CARDIOVOICE— 510(k) K952065

Substantially Equivalent

Paceart, Inc.

FDA 510(k) clearance K952065 for PACEART CARDIOVOICE, Substantially Equivalent on 1996-01-16. Applicant: Paceart, Inc..

Clearance details

Applicant: Paceart, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1995-05-02
Decision date: 1996-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, US

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