510(k) K860233 ยท HEM Imager, Ultrasonic Obstetric-Gynecologic
5 MHZ INTRACAVITARY PROBE, MODEL H4222V
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 2, 1986 |
| Received | Jan 22, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860233
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.