Clearance Summary
MODIFICATION TO THERMOFOCUS 0800, 0900, 01500 AND 0700 SERIES received FDA 510(k) clearance under submission number K072108, sponsored by Tecnimed S.R.L.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2007-08-31.
- Submission: K072108
- Applicant / Sponsor: Tecnimed S.R.L.
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2007-08-31
Classification & Regulation
This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.