510(k) K133861 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
FLASH OSTIAL SYSTEM OTW-7.0MMX17MMX135CM, FLASH OSTIAL SYSTEM OTW-7.0MMX17MMX80CM
| Applicant | Ostial Corporation, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Jul 2, 2014 |
| Received | Dec 19, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133861
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.