Clearance Summary
Bravo G4 Chamber Autoclave received FDA 510(k) clearance under submission number K210326, sponsored by Scican , Ltd.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2021-07-01.
- Submission: K210326
- Applicant / Sponsor: Scican , Ltd.
- Clearance pathway: Abbreviated
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6880
- Decision date: 2021-07-01
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.