Clearance Summary
Pulse Oximeter (Model C101A2, C101B1, C101A3) received FDA 510(k) clearance under submission number K221979, sponsored by Shenzhen Imdk Medical Technology Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2022-10-16.
- Submission: K221979
- Applicant / Sponsor: Shenzhen Imdk Medical Technology Co., Ltd.
- Clearance pathway: Special
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.2700
- Decision date: 2022-10-16
Classification & Regulation
This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.