The following data is part of a premarket notification filed by Mri Devices Corp. with the FDA for Kfa-12 Knee, Foot, And Ankle Array Coil.
| Device ID | K033151 |
| 510k Number | K033151 |
| Device Name: | KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL |
| Classification | Coil, Magnetic Resonance, Specialty |
| Applicant | MRI DEVICES CORP. 1515 PARAMOUNT DR. Waukesha, WI 53186 |
| Contact | Thomas Schubert |
| Correspondent | Thomas Schubert MRI DEVICES CORP. 1515 PARAMOUNT DR. Waukesha, WI 53186 |
| Product Code | MOS |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-30 |
| Decision Date | 2003-10-10 |