PACEART CARDIOPHONE— 510(k) K931296

Substantially Equivalent

Paceart, Inc.

FDA 510(k) clearance K931296 for PACEART CARDIOPHONE, Substantially Equivalent on 1993-10-01. Applicant: Paceart, Inc..

Clearance details

Applicant: Paceart, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1993-03-30
Decision date: 1993-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, US

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