510(k) K910669 ยท ITX Transducer, Ultrasonic, Diagnostic
5 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU
| Applicant | Siemens Ultrasound, Inc., San Ramon CA, US |
| Decision | Substantially Equivalent, Mar 15, 1991 |
| Received | Feb 15, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910669
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.