510(k) K122152 ยท MAV Syringe, Balloon Inflation
OXTI INFLATION DEVICE
| Applicant | Oxti Corporation, Houston TX, US |
| Decision | Substantially Equivalent, Dec 14, 2012 |
| Received | Jul 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122152
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.