Clearance Summary
ULTRAMAX/MODEL NUMBER A1 received FDA 510(k) clearance under submission number K960044, sponsored by Entlab OY. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-08-02.
- Submission: K960044
- Applicant / Sponsor: Entlab OY
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 1996-08-02
Classification & Regulation
This clearance is catalogued under FDA product code LWI and 21 CFR 892.1560, within the Radiology review panel as a Class II device.