510(k) K160178
K160178 is an FDA 510(k) premarket notification submitted by Daesung Maref Co., Ltd. for the device "Lympha-Flow(LF1200)". The FDA issued a decision of Substantially Equivalent on January 11, 2017. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Daesung Maref Co., Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 11, 2017
- Date Received
- January 27, 2016
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Massager, Powered Inflatable Tube
- Device Class
- Class II
- Regulation Number
- 890.5650
- Review Panel
- PM
- Submission Type