510(k) K875334 ยท HGL Transducer, Ultrasonic, Obstetric
KONTRON SIGMA 1 DIGITAL ECHOCARDIOGRAPH SYSTEM
| Applicant | Kontron Instruments, Inc., Everett MA, US |
| Decision | Substantially Equivalent, Mar 24, 1988 |
| Received | Dec 30, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K875334
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.