FDA 510(k)

CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR

K-Number: K990011 · 1999-05-11

Decision Date1999-05-11

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR is the device name listed in this FDA 510(k) record. The listed applicant is Continental Soft Lens, Inc.. It received FDA 510(k) clearance on 1999-05-11 under 510(k) number K990011. 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 CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR?

CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR is a medical device that received FDA 510(k) clearance on 1999-05-11. The listed applicant is Continental Soft Lens, Inc.. The 510(k) number is K990011.

When did CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR receive FDA 510(k) clearance?

CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR received FDA 510(k) clearance on 1999-05-11, under 510(k) number K990011.

Who is the listed applicant for CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR?

The FDA 510(k) record lists Continental Soft Lens, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR?

The FDA product code for CONTINENTAL 45 TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WEAR is LPL.

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Other records listing Continental Soft Lens, Inc. 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.