510(k) K961334 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
HEARTPORT HANDSWITCH ELECTROCAUTERY PROBE
| Applicant | Heartport, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Nov 15, 1996 |
| Received | Apr 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961334
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.