510(k) K993648 ยท MCW Catheter, Peripheral, Atherectomy
ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM WITH THE ROTALINK EXCHANGEABLE CATHETER
| Applicant | Boston Scientific Corporation Northwest Technology, Redmond WA, US |
| Decision | Substantially Equivalent, Nov 24, 1999 |
| Received | Oct 29, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K993648
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.