PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS— 510(k) K880283

Substantially Equivalent

Paceart, Inc.

FDA 510(k) clearance K880283 for PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS, Substantially Equivalent on 1988-03-09. Applicant: Paceart, Inc..

Clearance details

Applicant: Paceart, Inc.
Product code: Code DXH
Advisory panel: Cardiovascular
Date received: 1988-01-22
Decision date: 1988-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wayne, NJ, US

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