Clearance Summary
POD PAC-20M received FDA 510(k) clearance under submission number K030610, sponsored by Portable Ophthalmic Devices, 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 2003-03-21.
- Submission: K030610
- Applicant / Sponsor: Portable Ophthalmic Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2003-03-21
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.