Clearance Summary
VESSA TRAVVLA received FDA 510(k) clearance under submission number K853593, sponsored by Vessa , Ltd.. 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 1985-09-24.
- Submission: K853593
- Applicant / Sponsor: Vessa , Ltd.
- Clearance pathway: Traditional
- Review panel: Physical Medicine
- Device class: Class II
- Regulation citation: 21 CFR 890.3860
- Decision date: 1985-09-24
Classification & Regulation
This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.