Clearance Summary
Vicks RapidRead Digital Thermometer received FDA 510(k) clearance under submission number K180131, sponsored by Kaz USA, Inc., A Helen of Troy Company. 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 2018-08-14.
- Submission: K180131
- Applicant / Sponsor: Kaz USA, Inc., A Helen of Troy Company
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2018-08-14
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.