Clearance Summary
PROPPER INSIGHT BINOCULAR INDIRECT OPHTHALMOSOPE received FDA 510(k) clearance under submission number K141638, sponsored by Propper Manufacturing Co., Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 2014-09-17.
- Submission: K141638
- Applicant / Sponsor: Propper Manufacturing Co., Inc.
- Clearance pathway: Abbreviated
- Review panel: Ophthalmic
- Device class: Class II
- Regulation citation: 21 CFR 886.1570
- Decision date: 2014-09-17
Classification & Regulation
This clearance is catalogued under FDA product code HLI and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.