Clearance Summary
VISUCAM received FDA 510(k) clearance under submission number K021787, sponsored by Carl Zeiss Ophthalmic Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-06-21.
- Submission: K021787
- Applicant / Sponsor: Carl Zeiss Ophthalmic Systems, Inc.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class I
- Regulation citation: 21 CFR 892.2010
- Decision date: 2002-06-21
Classification & Regulation
This clearance is catalogued under FDA product code NFF and 21 CFR 892.2010, within the Radiology review panel as a Class I device.