510(k) K992120 ยท LNH System, Nuclear Magnetic Resonance Imaging
DYNAWELL OR DYNAWELL
| Applicant | Ekeroth Quality AB, Stockholm, SE |
| Decision | Substantially Equivalent, Aug 13, 1999 |
| Received | Jun 23, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992120
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.