Clearance Summary
SANICLAVE 200 received FDA 510(k) clearance under submission number K112811, sponsored by Alternative Pioneering Research and Development. 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 2012-01-11.
- Submission: K112811
- Applicant / Sponsor: Alternative Pioneering Research and Development
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6880
- Decision date: 2012-01-11
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.