510(k) K070612
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 7, 2007
- Date Received
- March 5, 2007
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Electrode, Cutaneous
- Device Class
- Class II
- Regulation Number
- 882.1320
- Review Panel
- NE
- Submission Type