Clearance Summary
VTS1000 received FDA 510(k) clearance under submission number K101838, sponsored by Vuetek Scientific, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2011-02-18.
- Submission: K101838
- Applicant / Sponsor: Vuetek Scientific, LLC
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class I
- Regulation citation: 21 CFR 880.6970
- Decision date: 2011-02-18
Classification & Regulation
This clearance is catalogued under FDA product code KZA and 21 CFR 880.6970, within the General Hospital review panel as a Class I device.