510(k) K000397 ยท FHN Ligator, Hemorrhoidal
SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODELS 4225, 4228; INJECTION SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODEL
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Mar 7, 2000 |
| Received | Feb 7, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000397
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.