510(k) K061732
K061732 is an FDA 510(k) premarket notification submitted by Airway Management, Inc. for the device "TAP-T". The FDA issued a decision of Substantially Equivalent on July 12, 2006. The device falls under product code LRK (Device, Anti-Snoring), a Class II device regulated under 21 CFR 872.5570. Airway Management, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 12, 2006
- Date Received
- June 20, 2006
- Clearance Type
- Special
- 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