510(k) K972379 ยท DXQ Blood Pressure Cuff
PRECISA N
| Applicant | Rudolf Riester GmbH & Co. KG, Jungingen, DE |
| Decision | Substantially Equivalent, Sep 24, 1997 |
| Received | Jun 26, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972379
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.