510(k) K022532 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
TISSUELINK BIPOLAR FLOATING BALL DEVICE
| Applicant | Tissuelink Medical, Inc., Dover NH, US |
| Decision | Substantially Equivalent, Feb 12, 2003 |
| Received | Jul 31, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022532
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 1, 2004 | TissueLink Medical, Inc. ADP2.1 Adapter, non-sterile reusable
Model Number: 30-802-1 ,an accessory used with the TissueLink BiPolar Floating Device Terminated |
GEI | None listed |
| Sep 1, 2004 | TissueLink Medical, Inc. ADP 3.2 Adapter, non sterile reusable
Model Number: 30-801-1, an accessory used with the TissueLink Bipolar Floating Device Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.