FDA 510(k)

MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR

K-Number: K021720 · 2002-08-12

ApplicantSoflex Isralens Contact Lens , Ltd.

Decision Date2002-08-12

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR is the device name listed in this FDA 510(k) record. The listed applicant is Soflex Isralens Contact Lens , Ltd.. It received FDA 510(k) clearance on 2002-08-12 under 510(k) number K021720. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR?

MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR is a medical device that received FDA 510(k) clearance on 2002-08-12. The listed applicant is Soflex Isralens Contact Lens , Ltd.. The 510(k) number is K021720.

When did MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR receive FDA 510(k) clearance?

MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR received FDA 510(k) clearance on 2002-08-12, under 510(k) number K021720.

Who is the listed applicant for MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR?

The FDA 510(k) record lists Soflex Isralens Contact Lens , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR?

The FDA product code for MULTIVISION METHAFILCON A SOFT (HYDROPILIC) MULTIFOCAL LENS FOR DAILY WEAR is LPL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.