The following data is part of a premarket notification filed by Midwest R.f. Llc. with the FDA for Special Procedures Ii Head Coil, Model 1400ge-64.
Device ID | K051618 |
510k Number | K051618 |
Device Name: | SPECIAL PROCEDURES II HEAD COIL, MODEL 1400GE-64 |
Classification | Coil, Magnetic Resonance, Specialty |
Applicant | MIDWEST R.F. LLC. 535 NORTON DR. P.O. BOX 348 Hartland, WI 53029 |
Contact | David M Peterson |
Correspondent | David M Peterson 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 | 2005-06-17 |
Decision Date | 2005-08-02 |