Clearance Summary
VAPOTHERM MODEL# 2000I AND 2000H received FDA 510(k) clearance under submission number K070056, sponsored by Vapotherm, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2007-04-13.
- Submission: K070056
- Applicant / Sponsor: Vapotherm, Inc.
- Clearance pathway: Special
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5450
- Decision date: 2007-04-13
Classification & Regulation
This clearance is catalogued under FDA product code BTT and 21 CFR 868.5450, within the Anesthesiology review panel as a Class II device.