HRK-123 KNEE ARRAY COIL— 510(k) K050299
Substantially EquivalentMri Devices Corporation
FDA 510(k) clearance K050299 for HRK-123 KNEE ARRAY COIL, Substantially Equivalent on 2005-02-24. Applicant: Mri Devices Corporation. Device class: 2.
Clearance details
- Applicant
- Mri Devices Corporation
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Pewaukee, WI, US
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More clearances from Mri Devices Corporation
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