510(k) K042538 ยท DQY Catheter, Percutaneous
SAILOR PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL SAEXXXXXXXXX
| Applicant | Invatec Innovative Technologies, Plymouth MN, US |
| Decision | Substantially Equivalent, Nov 8, 2004 |
| Received | Sep 20, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042538
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.