510(k) K230722
K230722 is an FDA 510(k) premarket notification submitted by Belkin Vision, Ltd. for the device "Eagle device". The FDA issued a decision of Substantially Equivalent on December 8, 2023. The device falls under product code HQF (Laser, Ophthalmic), a Class II device regulated under 21 CFR 886.4390. Belkin Vision, Ltd. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 8, 2023
- Date Received
- March 16, 2023
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laser, Ophthalmic
- Device Class
- Class II
- Regulation Number
- 886.4390
- Review Panel
- OP
- Submission Type