510(k) K200724
K200724 is an FDA 510(k) premarket notification submitted by Technolas Perfect Vision GmbH for the device "VICTUS Femtosecond Laser Platform". The FDA issued a decision of Substantially Equivalent on September 1, 2020. The device falls under product code OOE (Ophthalmic Femtosecond Laser), a Class II device regulated under 21 CFR 886.4390. Technolas Perfect Vision GmbH has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 1, 2020
- Date Received
- March 19, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ophthalmic Femtosecond Laser
- Device Class
- Class II
- Regulation Number
- 886.4390
- Review Panel
- OP
- Submission Type
Precise cutting or ablation of ocular tissue, indicated for the anterior capsulotomy during cataract surgery.