Clearance Summary
Digital Thermometer received FDA 510(k) clearance under submission number K182629, sponsored by Joytech Healthcare 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 2019-02-28.
- Submission: K182629
- Applicant / Sponsor: Joytech Healthcare Co. , Ltd.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2019-02-28
Classification & Regulation
This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.