510(k) K242391
K242391 is an FDA 510(k) premarket notification submitted by Lucens Technology Co., Ltd. for the device "Lucens 41 (senofilcon C) Silicone Hydrogel Soft (Hydrophilic) Contact Lens". The FDA issued a decision of Substantially Equivalent on Oct 8, 2024. The device falls under product code LPL (Lenses, Soft Contact, Daily Wear), a Class II device regulated under 21 CFR 886.5925.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 8, 2024
- Date Received
- Aug 12, 2024
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lenses, Soft Contact, Daily Wear
- Device Class
- Class II
- Regulation Number
- 886.5925
- Review Panel
- OP
- Submission Type