Clearance Summary
MICROLIFE DUAL MODE THERMOMETER,MODEL IFR1MJ1 received FDA 510(k) clearance under submission number K113141, sponsored by Microlife Intellectual Property GmbH. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2012-01-27.
- Submission: K113141
- Applicant / Sponsor: Microlife Intellectual Property GmbH
- Clearance pathway: Special
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2012-01-27
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.