510(k) K003880 ยท DQY Catheter, Percutaneous
CONCENTROC HD GUIDE CATHETER, MODELS 90017 (4F), 90019 (5F), 90021 (6F), 90022 (7F), 90023 (8F), 90024 (9F)
| Applicant | Concentric Medical, Inc., Moutian View CA, US |
| Decision | Substantially Equivalent, May 16, 2001 |
| Received | Dec 15, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K003880
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.