The following data is part of a premarket notification filed by Midwest R.f. Llc. with the FDA for Brain Coil, Model 9800ge-64.
Device ID | K003097 |
510k Number | K003097 |
Device Name: | BRAIN COIL, MODEL 9800GE-64 |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | MIDWEST R.F. LLC. 535 NORTON DR. P.O. BOX 348 Hartland, WI 53029 |
Contact | Ralph S Hashoian |
Correspondent | Ralph S Hashoian MIDWEST R.F. LLC. 535 NORTON DR. P.O. BOX 348 Hartland, WI 53029 |
Product Code | MOS |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-10-03 |
Decision Date | 2000-12-28 |