510(k) K072332 ยท GEX Powered Laser Surgical Instrument
VARI-LASE WIRE FIBER
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 10, 2008 |
| Received | Aug 20, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072332
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 3, 2011 | Vascular Solutions, Inc. Vari Lase WireFiber Laser Fiber, RED 7137, Rx ONLY, Sterile EO, Vascular Solutions Inc., 6464 Sycamore Court, Minneapolis, MN 55369
The VARI-LASE WireFiber is indicated for the treatment of varicose Terminated |
GEX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.