510(k) K010213 ยท ETN Stimulator, Nerve
MODIFICATION TO CAVERMAP SURGICAL AID
| Applicant | Uromed Corp., Norwood MA, US |
| Decision | Substantially Equivalent, Apr 20, 2001 |
| Received | Jan 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010213
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.