510(k) K131450 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
FLASH MINI OSTIAL SYSTEM - 3.0MM X 135CM, FLASH MINI OSTIAL SYSTEM - 3.5MM X 8MM X 135CM, FLASH MINI OSTIAL SYSTEM - 4.0
| Applicant | Ostial Corporation, Mountain View CA, US |
| Decision | Substantially Equivalent, Aug 6, 2013 |
| Received | May 20, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131450
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.