FDA 510(k)

LL-55 (METHAFILCON A) FOR DAILY WEAR

K-Number: K941877 · 1994-06-14

Decision Date1994-06-14

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

LL-55 (METHAFILCON A) FOR DAILY WEAR is the device name listed in this FDA 510(k) record. The listed applicant is Lombart Lenses, Ltd.. It received FDA 510(k) clearance on 1994-06-14 under 510(k) number K941877. 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 LL-55 (METHAFILCON A) FOR DAILY WEAR?

LL-55 (METHAFILCON A) FOR DAILY WEAR is a medical device that received FDA 510(k) clearance on 1994-06-14. The listed applicant is Lombart Lenses, Ltd.. The 510(k) number is K941877.

When did LL-55 (METHAFILCON A) FOR DAILY WEAR receive FDA 510(k) clearance?

LL-55 (METHAFILCON A) FOR DAILY WEAR received FDA 510(k) clearance on 1994-06-14, under 510(k) number K941877.

Who is the listed applicant for LL-55 (METHAFILCON A) FOR DAILY WEAR?

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

What is the FDA product code for LL-55 (METHAFILCON A) FOR DAILY WEAR?

The FDA product code for LL-55 (METHAFILCON A) FOR DAILY WEAR is LPL.

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Other records listing Lombart Lenses, Ltd. as applicant

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Related Devices (Code: LPL)

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.