Clearance Summary
STERLINKTM FPS-15s Plus Sterilizer with STERLOADTM Cassette received FDA 510(k) clearance under submission number K212200, sponsored by Plasmapp Co,., 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 2021-10-22.
- Submission: K212200
- Applicant / Sponsor: Plasmapp Co,., Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.6860
- Decision date: 2021-10-22
Classification & Regulation
This clearance is catalogued under FDA product code MLR and 21 CFR 880.6860, within the General Hospital review panel as a Class II device.