FDA 510(k)

LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)

K-Number: K991015 · 1999-11-02

Decision Date1999-11-02

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) is the device name listed in this FDA 510(k) record. The listed applicant is Lamda Polytech , Ltd.. It received FDA 510(k) clearance on 1999-11-02 under 510(k) number K991015. 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 LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)?

LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) is a medical device that received FDA 510(k) clearance on 1999-11-02. The listed applicant is Lamda Polytech , Ltd.. The 510(k) number is K991015.

When did LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) receive FDA 510(k) clearance?

LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) received FDA 510(k) clearance on 1999-11-02, under 510(k) number K991015.

Who is the listed applicant for LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)?

The FDA 510(k) record lists Lamda Polytech , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT)?

The FDA product code for LM-70 (LIDOFILCON A) SPHERICAL AND TORIC SOFT CONTACT LENS FOR DAILY WEAR (CLEAR, LATHE-CUT) 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.