The following data is part of a premarket notification filed by Philips Medical Systems North America, Inc. with the FDA for Philips Ct Secura Mv.
| Device ID | K000819 |
| 510k Number | K000819 |
| Device Name: | PHILIPS CT SECURA MV |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Contact | Frank Gianelli |
| Correspondent | Frank Gianelli PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-03-13 |
| Decision Date | 2000-05-12 |