Company ยท US
Cardiac Pathways Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2000. Name variants (Inc, Corp, punctuation) are merged.
5510(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 |
|---|---|---|---|
| Mar 8, 2000 | K992912 | CARDIAC PATHWAYS REFERENCE CATHETER AND REFERENCE CATHETER WITH TRACKING, CARDIAC PATHWAYS RADII CATHETER AND RADII CATH Cardiac Pathways Corp. | DRF |
| Jun 8, 1999 | K990795 | MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER; CARDIAC PATHWAYS EGM ADAPTER CABLES Cardiac Pathways Corp. | MTD |
| Jan 27, 1999 | K982540 | MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER MODELS, 7005, 7006, 7007, MERCATOR ATRIAL HIGH DENSITY ARRAY DEPLOYMENT KIT, Cardiac Pathways Corp. | MTD |
| Dec 22, 1998 | K983653 | RADII DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER, MODEL # 30411 B, C AND D Cardiac Pathways Corp. | DRF |
| Aug 11, 1997 | K965066 | ARRHYTHMIA MAPPING SYSTEM (8100/8300) Cardiac Pathways Corp. | DRF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||