510(k) K852655 ยท KNG Monitor, Ultrasonic, Fetal
COMBISCOPE
| Applicant | Instrument Technology, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Feb 21, 1986 |
| Received | Jun 24, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852655
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.