Clearance Summary
MODEL 555 010 XY CONVERSION(55010) received FDA 510(k) clearance under submission number K960737, sponsored by Systems Supply Services, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1996-05-22.
- Submission: K960737
- Applicant / Sponsor: Systems Supply Services, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5840
- Decision date: 1996-05-22
Classification & Regulation
This clearance is catalogued under FDA product code KPQ and 21 CFR 892.5840, within the Radiology review panel as a Class II device.