510(k) K923343 ยท DQA Oximeter
HEWLETT-PACKARD MODEL M1020A PULSE OXIMETER
| Applicant | Hewlett-Packard Co., Germany, DE |
| Decision | Substantially Equivalent, Feb 10, 1993 |
| Received | Jun 18, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923343
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.