510(k) K062455 ยท DQA Oximeter
PHILIPS ADULT REUSABLE SP02 SENSOR, MODEL M1191B, M1191BL, M1191BNL
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Nov 3, 2006 |
| Received | Aug 23, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062455
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.