510(k) K982540 ยท MTD Catheter, Intracardiac Mapping, High-Density Array
MERCATOR ATRIAL HIGH DENSITY ARRAY CATHETER MODELS, 7005, 7006, 7007, MERCATOR ATRIAL HIGH DENSITY ARRAY DEPLOYMENT KIT,
| Applicant | Cardiac Pathways Corp., Sunnyvale CA, US |
| Decision | Unknown, Jan 27, 1999 |
| Received | Jul 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982540
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.