510(k) K960044 ยท LWI Ultrasound, Sinus
ULTRAMAX/MODEL NUMBER A1
| Applicant | Entlab OY, Richmond, CA |
| Decision | Substantially Equivalent, Aug 2, 1996 |
| Received | Jan 2, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960044
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.