The following data is part of a premarket notification filed by Philips Medical Systems North America, Inc. with the FDA for Philips Bucky Diagnost Family.
| Device ID | K945278 |
| 510k Number | K945278 |
| Device Name: | PHILIPS BUCKY DIAGNOST FAMILY |
| Classification | System, X-ray, Stationary |
| Applicant | PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Contact | Peter Altman |
| Correspondent | Peter Altman PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Product Code | KPR |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-10-28 |
| Decision Date | 1994-12-14 |