510(k) K103076
K103076 is an FDA 510(k) premarket notification submitted by Dyna Flex for the device "DYNAFLEX". The FDA issued a decision of Substantially Equivalent on February 23, 2011. The device falls under product code LRK (Device, Anti-Snoring), a Class II device regulated under 21 CFR 872.5570. Dyna Flex has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 23, 2011
- Date Received
- October 18, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Anti-Snoring
- Device Class
- Class II
- Regulation Number
- 872.5570
- Review Panel
- DE
- Submission Type