510(k) K070485 ยท DXC Clamp, Vascular
BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L
| Applicant | Cardiva Medical, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Mar 22, 2007 |
| Received | Feb 20, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K070485
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.