Cleared Traditional

K000164 - COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION
(FDA 510(k) Clearance)

Jun 2000
Decision
135d
Days
Class 2
Risk

K000164 is an FDA 510(k) clearance for the COMPLETE BRAND COMFORTPLUS MULTI-PURPOSE SOLUTION. This device is classified as a Accessories, Soft Lens Products (Class II - Special Controls, product code LPN).

Submitted by Allergan, Inc. (Irvine, US). The FDA issued a Cleared decision on June 2, 2000, 135 days after receiving the submission on January 19, 2000.

This device falls under the Ophthalmic FDA review panel. Regulated under 21 CFR 886.5928.

Submission Details

510(k) Number K000164 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 19, 2000
Decision Date June 02, 2000
Days to Decision 135 days
Submission Type Traditional
Review Panel Ophthalmic (OP)
Summary Summary PDF

Device Classification

Product Code LPN — Accessories, Soft Lens Products
Device Class Class II - Special Controls
CFR Regulation 21 CFR 886.5928

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