510(k) K851848 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
PERCUTANEOUS TRANSLUMINAL BLOOD DILATION CATHETER
| Applicant | Mansfield Scientific, Inc., Mansfield MA, US |
| Decision | Substantially Equivalent, Jul 19, 1985 |
| Received | Apr 26, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K851848
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.