The following data is part of a premarket notification filed by Philips Medizin Systeme Boblingen Gmbh with the FDA for Philips M3001a Multi Measurement Server.
| Device ID | K090360 |
| 510k Number | K090360 |
| Device Name: | PHILIPS M3001A MULTI MEASUREMENT SERVER |
| Classification | Oximeter |
| Applicant | PHILIPS MEDIZIN SYSTEME BOBLINGEN GMBH HEWLETT-PACKARD-STR. 2 Boblingen, DE D-71034 |
| Contact | Jens-peter Seher |
| Correspondent | Jens-peter Seher PHILIPS MEDIZIN SYSTEME BOBLINGEN GMBH HEWLETT-PACKARD-STR. 2 Boblingen, DE D-71034 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-02-12 |
| Decision Date | 2009-05-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838000254 | K090360 | 000 |