510(k) K083162 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
STINGRAY ELECTROSURGICAL FORCEPS
| Applicant | Stingray Surgical Products, Inc., Deer Field IL, US |
| Decision | Substantially Equivalent, Jan 12, 2009 |
| Received | Oct 27, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083162
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 13, 2012 | Stingray Surgical Products, LLC Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX. "Instructions For Use" (QF7.5.1A.R01 thru QF7.5.1A.R06 Care and Handling of Bipolar Forceps.
Bipolar Forceps designed to grasp, Terminated |
GEI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.