510(k) K202448

DAILIES AquaComfort Plus (DACP) / DACP FreshTech / DACP Toric / DACP Multifocal by Alcon Laboratories, Inc. — Product Code MVN

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