Clearance Summary
KENSTONE received FDA 510(k) clearance under submission number K990139, sponsored by Kenda USA. 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 1999-04-29.
- Submission: K990139
- Applicant / Sponsor: Kenda USA
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class I
- Regulation citation: 21 CFR 890.3850
- Decision date: 1999-04-29
Classification & Regulation
This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.