510(k) K010883 ยท ITX Transducer, Ultrasonic, Diagnostic
TERATECH MODEL 8EC4 ENDOCAVITY SMART PROBE
| Applicant | Teratech Corp., Saratoga CA, US |
| Decision | Substantially Equivalent, Apr 6, 2001 |
| Received | Mar 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010883
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.