510(k) K881136 ยท DQA Oximeter
HEWLETT-PACKARD MODELS 78354A & 78352A PULSE OXI.
| Applicant | Hewlett-Packard Co., Waltham MA, US |
| Decision | Substantially Equivalent, May 18, 1988 |
| Received | Mar 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881136
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.