510(k) K073057 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PULSAR GENERATOR, MODEL PS100-100, AND PEAK PLASMABLADE TISSUE DISSECTION DEVICE, MODEL PS200-040
| Applicant | Peak Surgical, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jul 22, 2008 |
| Received | Oct 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073057
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.