510(k) K991830 ยท JOS Electrode, Electrosurgical
CAPSULAR SHRINKAGE ELECTRODE
| Applicant | Linvatec Corp., Largo FL, US |
| Decision | Substantially Equivalent, Aug 20, 1999 |
| Received | May 28, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991830
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 29, 2016 | ConMed Corporation CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only
Product Usage:
The HeatWave Electrode is intended to be used for electro-coagulation of soft tissue in Terminated |
JOS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.