Clearance Summary
Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves received FDA 510(k) clearance under submission number K181456, sponsored by Tuttnauer , Ltd.. 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 2019-07-08.
- Submission: K181456
- Applicant / Sponsor: Tuttnauer , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6880
- Decision date: 2019-07-08
Classification & Regulation
This clearance is catalogued under FDA product code FLE and 21 CFR 880.6880, within the General Hospital review panel as a Class II device.