510(k) K100801 ยท IYE Accelerator, Linear, Medical
PUMA MODEL VERSION 1.0
| Applicant | Prowess, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Jun 18, 2010 |
| Received | Mar 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100801
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.