The following data is part of a premarket notification filed by Philips Medical Systems North America, Inc. with the FDA for Philips Gyroscan T5 Series Ii.
| Device ID | K920578 |
| 510k Number | K920578 |
| Device Name: | PHILIPS GYROSCAN T5 SERIES II |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Contact | William G Mcmahon |
| Correspondent | William G Mcmahon PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC. 710 BRIDGEPORT AVE. Shelton, CT 06484 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-10 |
| Decision Date | 1992-11-06 |