Clearance Summary
JASUN, MODELS DT-01F AND DT-11F received FDA 510(k) clearance under submission number K030361, sponsored by Hangzhou Hua'An Medical & Health Instruments Co.,. 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 2003-02-21.
- Submission: K030361
- Applicant / Sponsor: Hangzhou Hua'An Medical & Health Instruments Co.,
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.2910
- Decision date: 2003-02-21
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.