510(k) K071244 ยท DXQ Blood Pressure Cuff
MEDLINE SINGLE PATIENT USE BLOOD PRESSURE CUFF
| Applicant | Medline Industries, Inc., Mundelein IL, US |
| Decision | Substantially Equivalent, Mar 5, 2008 |
| Received | May 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071244
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.