The following data is part of a premarket notification filed by Hitachi Medical Systems America, Inc. with the FDA for Airis Elite Magnetic Resonance Imaging Device.
| Device ID | K032232 |
| 510k Number | K032232 |
| Device Name: | AIRIS ELITE MAGNETIC RESONANCE IMAGING DEVICE |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | HITACHI MEDICAL SYSTEMS AMERICA, INC. 1959 SUMMIT COMMERCE PARK Twinsburg, OH 44087 |
| Contact | Douglas Thistlethwaite |
| Correspondent | Douglas Thistlethwaite HITACHI MEDICAL SYSTEMS AMERICA, INC. 1959 SUMMIT COMMERCE PARK Twinsburg, OH 44087 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-07-21 |
| Decision Date | 2003-09-29 |
| Summary: | summary |