Clearance Summary
VISIONLINK ACR-NEMA CONVERSION UTILITIES received FDA 510(k) clearance under submission number K935103, sponsored by Evergreen Technologies, 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 1994-02-09.
- Submission: K935103
- Applicant / Sponsor: Evergreen Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.2020
- Decision date: 1994-02-09
Classification & Regulation
This clearance is catalogued under FDA product code LMD and 21 CFR 892.2020, within the Radiology review panel as a Class I device.