510(k) K202044
K202044 is an FDA 510(k) premarket notification submitted by Hanuri Distribution, Inc. for the device "Powerpress Recovery Unit". The FDA issued a decision of Substantially Equivalent on Oct 21, 2020. The device falls under product code IRP (Massager, Powered Inflatable Tube), a Class II device regulated under 21 CFR 890.5650. Hanuri Distribution, Inc. has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 21, 2020
- Date Received
- Jul 23, 2020
- Clearance Type
- Traditional
- 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
- 510(k)