510(k) K905101 ยท DXQ Blood Pressure Cuff
NEONATAL/STERILE/DISPOS/NONINVAS BLOOD PRESS CUFF
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Dec 20, 1990 |
| Received | Nov 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905101
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.