510(k) K110750
K110750 is an FDA 510(k) premarket notification submitted by Mis Implants Technologies , Ltd. for the device "PERIOPATCH". The FDA issued a decision of Substantially Equivalent on Apr 28, 2011. The device falls under product code OLR (Oral Wound Dressing), a Class U device. Mis Implants Technologies , Ltd. has 12 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 28, 2011
- Date Received
- Mar 17, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Oral Wound Dressing
- Device Class
- Class U
- Review Panel
- DE
- Submission Type
- 510(k)
Intended as a physical barrier for temporary protection of oral mucosal tissue and to provide pain relief. Unclassified status per SE to MGQ.