510(k) K121272
K121272 is an FDA 510(k) premarket notification submitted by Akervall Technologies, Inc. for the device "PROTECH DENT". The FDA issued a decision of Substantially Equivalent on Oct 15, 2012. The device falls under product code OBR (Mouthguard, Over-The-Counter), a Class U device.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 15, 2012
- Date Received
- Apr 27, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mouthguard, Over-The-Counter
- Device Class
- Class U
- Review Panel
- DE
- Submission Type
- 510(k)
To protect the teeth and reduce damage caused by bruxing or nighttime grinding and prevention of the noise associated with bruxing and grinding.