Company ยท US
Paceart, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 2001. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 14, 2001 | K012407 | PACEART TX3 CARDIAC EVENT RECORDER Paceart, Inc. | DXH |
| Jan 26, 1999 | K982090 | PACEART HOME TRAK PLUS EASI EVENT RECORDER SYSTEM Paceart, Inc. | DXH |
| Nov 12, 1997 | K973141 | HEART ACCESS PLUS CARDIAC EVENT RECORDER Paceart, Inc. | DXH |
| Jul 18, 1996 | K960721 | PACEART WRIST ELECTRODES Paceart, Inc. | DRX |
| Jan 16, 1996 | K952065 | PACEART CARDIOVOICE Paceart, Inc. | DXH |
| Oct 1, 1993 | K931296 | PACEART CARDIOPHONE Paceart, Inc. | DXH |
| Apr 14, 1992 | K915632 | PACEART CPTS-86/12 Paceart, Inc. | KRE |
| Mar 9, 1988 | K880283 | PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS Paceart, Inc. | DXH |
| Apr 27, 1987 | K870909 | PACEMAKER FUNCTION ANALYZER Paceart, Inc. | KRE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||