510(k) K013732
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 2002
- Date Received
- November 9, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Elastomer, Silicone, For Scar Management
- Device Class
- Class I
- Regulation Number
- 878.4025
- Review Panel
- SU
- Submission Type