The following data is part of a premarket notification filed by Philips Medical Systems Nederland B.v. with the FDA for Brain Perfusion (bp) Application.
| Device ID | K182716 |
| 510k Number | K182716 |
| Device Name: | Brain Perfusion (BP) Application |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Philips Medical Systems Nederland B.V. Veenpluis 4-6 Best Noord-brabant, NL 5684 Pc |
| Contact | Yoram Levy |
| Correspondent | Yoram Levy Qsite 31 Haavoda St. Binyamina, IL 30500 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-09-27 |
| Decision Date | 2019-05-29 |