Clearance Summary
D-Actor 200 Vibration Massage System received FDA 510(k) clearance under submission number K173692, sponsored by Storz Medical AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2018-04-13.
- Submission: K173692
- Applicant / Sponsor: Storz Medical AG
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.5660
- Decision date: 2018-04-13
Classification & Regulation
This clearance is catalogued under FDA product code ISA and 21 CFR 890.5660, within the Physical Medicine review panel as a Class I device.