510(k) K133852 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
APOLLO BALLOON DILATATION CATHETER
| Applicant | Brosmed Medical, Dongguan, Guangdong, CN |
| Decision | Substantially Equivalent, Sep 19, 2014 |
| Received | Dec 19, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133852
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.