510(k) K081937 ยท DQA Oximeter
PICOSAT II AND M3002A MULTIMEASUREMENT AND M1020B PLUG-IN MODULES SPO2 PULSE OXIMETRY MODULE
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Bw, DE |
| Decision | Substantially Equivalent, Aug 29, 2008 |
| Received | Jul 7, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081937
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.