510(k) K853702 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ULTRASOUND COUPLANT SHEET/SOLID ULTRASOUND COUPLAN
| Applicant | Johnson & Johnson Professionals, Inc., Ramsey NJ, US |
| Decision | Substantially Equivalent, Feb 13, 1986 |
| Received | Sep 4, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853702
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.