510(k) K860102 ยท FHP Needle, Pneumoperitoneum, Simple
MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE
| Applicant | Endotherapeutics, Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 12, 1986 |
| Received | Jan 10, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860102
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.