510(k) K934180 ยท DXQ Blood Pressure Cuff
SLIMLINE 3000
| Applicant | Pymah Corp., Potomac MD, US |
| Decision | Substantially Equivalent, Nov 24, 1993 |
| Received | Aug 27, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934180
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.