510(k) K990723 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
DYONICS VARICOSE VEIN ABLATION BLADE
| Applicant | Smith & Nephew, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Oct 5, 1999 |
| Received | Mar 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990723
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division TriVex 100SV Resector Kit, 4.5
Part Number: 7205876 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division TriVex 200LV Resector Kit, 5.5
Part Number: 7209271 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division 4.5 mm TRIVEX System Resector Kit (blade and tubing), 3 per box
Part Number: 7209514 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division 5.5 mm TRIVEX System Resector Kit (blade and tubing), 3 per box
Part Number: 7209515 Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.