The following data is part of a premarket notification filed by Ge Healthcare with the FDA for Ct Perfusion 4.
| Device ID | K052839 |
| 510k Number | K052839 |
| Device Name: | CT PERFUSION 4 |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | GE HEALTHCARE 3000 N. GRANDVIEW BLVD Waukesha, WI 53188 |
| Contact | Larry Kroger |
| Correspondent | Daniel W Lehtonen INTERTEK TESTING SERVICES 70 CODMAN HILL RD. Boxborough, MA 01719 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2005-10-07 |
| Decision Date | 2006-03-10 |
| Summary: | summary |