510(k) K100490 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
LITEPAC, MODEL 682
| Applicant | ClearStream Technologies , Ltd., Wexford, IE |
| Decision | Substantially Equivalent, Mar 16, 2010 |
| Received | Feb 19, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K100490
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.