HRH-63 HEAD ARRAY COIL
FDA 510(k) clearance K002774 · decided 2000-11-16
Clearance details
- K-number
- K002774
- Device name
- HRH-63 HEAD ARRAY COIL
- Applicant
- Mri Devices Corp.
- Decision
- Substantially Equivalent
- Date received
- 2000-09-06
- Decision date
- 2000-11-16
- Days to decision
- 71 days
- Clearance type
- Traditional
- Product code
- MOS
- Device class
- 2
- Regulation number
- 892.1000
- Medical specialty
- Radiology
- Advisory committee
- Radiology
- Location
- Waukesha, WI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.