510(k) K860009 ยท ITX Transducer, Ultrasonic, Diagnostic
5.0 MHZ MERIDIAN ULTRASOUND IMAGING SYSTEM
| Applicant | Johnson & Johnson Professionals, Inc., Ramsey NJ, US |
| Decision | Substantially Equivalent, Aug 20, 1986 |
| Received | Jan 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860009
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.