510(k) K130487 ยท FMI Needle, Hypodermic, Single Lumen
FASTRESPONDER STERNAL INTRAOSSEOUS DEVICE
| Applicant | Pyng Medical Corp., Richmond, Bc, CA |
| Decision | Substantially Equivalent, Jun 25, 2013 |
| Received | Feb 25, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130487
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.