510(k) K854743 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
2.5 MHZ PHASED ARRAY SECTOR MERIDIAN PROBE
| Applicant | Johnson & Johnson Professionals, Inc., Ramsey NJ, US |
| Decision | Substantially Equivalent, Feb 28, 1986 |
| Received | Nov 25, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854743
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.