510(k) K031675 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
SMITH & NEPHEW DYONICS ELECTROBLADE RESECTOR
| Applicant | Smith & Nephew, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Jun 20, 2003 |
| Received | May 30, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031675
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division Dyonics Electroblade, 4.5 Full Radius, Valleylab Generator-Compatible
Part Number: 7205961 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division Dyonics Electroblade 4.5 ELITE, Full Radius, Valleylab Generator- Compatible
Part Number: 7209700 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division Dyonics Electroblade 4.5 Full Radius, VULCAN Generator-Compatible
Product number: 7209855 Terminated |
GEI | None listed |
| Jul 13, 2006 | Smith & Nephew, Inc. Endoscopy Division Dyonics Electroblade 4.5 ELITE, Full Radius, VULCAN Generator-Compatible
Part Number: 7209983 Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.