510(k) K903523 ยท DQA Oximeter
HP MODEL M1020A, ARTERIAL OXYGEN SAT/PLETH MODULE
| Applicant | Hewlett-Packard Co., Germany, DE |
| Decision | Substantially Equivalent, Oct 23, 1990 |
| Received | Aug 6, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K903523
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.