Clearance Summary
MEDGRAPHIX INTL VR 1000 SERIES received FDA 510(k) clearance under submission number K921381, sponsored by Medgraphix Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1992-11-02.
- Submission: K921381
- Applicant / Sponsor: Medgraphix Intl.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2040
- Decision date: 1992-11-02
Classification & Regulation
This clearance is catalogued under FDA product code LMC and 21 CFR 892.2040, within the Radiology review panel as a Class II device.