510(k) K102029 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
PEAK PULSAR II GENERATOR MODEL PS100-102
| Applicant | Peak Surgical, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Dec 16, 2010 |
| Received | Jul 19, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102029
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.