The following data is part of a premarket notification filed by Philips Medical Systems with the FDA for Philips Cs770 Intellispace Critical Care And Anesthesia.
| Device ID | K151366 |
| 510k Number | K151366 |
| Device Name: | Philips CS770 IntelliSpace Critical Care And Anesthesia |
| Classification | Display, Cathode-ray Tube, Medical |
| Applicant | PHILIPS MEDICAL SYSTEMS 3000 MINUTEMAN ROAD Andover, MA 01810 |
| Contact | Kristen Phillips |
| Correspondent | Kristen Phillips PHILIPS MEDICAL SYSTEMS 3000 MINUTEMAN ROAD Andover, MA 01810 |
| Product Code | DXJ |
| CFR Regulation Number | 870.2450 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-05-21 |
| Decision Date | 2015-10-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00884838084674 | K151366 | 000 |
| 00884838085305 | K151366 | 000 |