510(k) K202448
K202448 is an FDA 510(k) premarket notification submitted by Alcon Laboratories, Inc. for the device "DAILIES AquaComfort Plus (DACP) / DACP FreshTech / DACP Toric / DACP Multifocal". The FDA issued a decision of Substantially Equivalent on September 22, 2020. The device falls under product code MVN (Lens, Contact, (Disposable)), a Class II device regulated under 21 CFR 886.5925. Alcon Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 22, 2020
- Date Received
- August 26, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Contact, (Disposable)
- Device Class
- Class II
- Regulation Number
- 886.5925
- Review Panel
- OP
- Submission Type