Clearance Summary
PC-DISPLAY received FDA 510(k) clearance under submission number K862309, sponsored by Hi-Tech Medical Systems, 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 1986-11-12.
- Submission: K862309
- Applicant / Sponsor: Hi-Tech Medical Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 1986-11-12
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.