510(k) K003719 ยท DWX Stripper, Artery, Intraluminal
VASCULAR ARCHITECTS PERISCOPE DEVICE
| Applicant | Vascular Architects, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Feb 28, 2001 |
| Received | Dec 4, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003719
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.