510(k) K130277
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 31, 2013
- Date Received
- February 4, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Densitometer, Bone
- Device Class
- Class II
- Regulation Number
- 892.1170
- Review Panel
- RA
- Submission Type