510(k) K111680
K111680 is an FDA 510(k) premarket notification submitted by Always More Marketing, Inc. for the device "DR. GREENSBURG'S HYBRID". The FDA issued a decision of Substantially Equivalent on Dec 23, 2011. The device falls under product code LRK (Device, Anti-Snoring), a Class II device regulated under 21 CFR 872.5570. Always More Marketing, Inc. has 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Dec 23, 2011
- Date Received
- Jun 15, 2011
- Clearance Type
- Abbreviated
- 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
- 510(k)