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Paceart, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K012407 PACEART TX3 CARDIAC EVENT RECORDERDXH2001-08-14 View
510(k) K982090 PACEART HOME TRAK PLUS EASI EVENT RECORDER SYSTEMDXH1999-01-26 View
510(k) K973141 HEART ACCESS PLUS CARDIAC EVENT RECORDERDXH1997-11-12 View
510(k) K960721 PACEART WRIST ELECTRODESDRX1996-07-18 View
510(k) K952065 PACEART CARDIOVOICEDXH1996-01-16 View
510(k) K931296 PACEART CARDIOPHONEDXH1993-10-01 View
510(k) K915632 PACEART CPTS-86/12KRE1992-04-14 View
510(k) K880283 PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTSDXH1988-03-09 View
510(k) K870909 PACEMAKER FUNCTION ANALYZERKRE1987-04-27 View
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