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FDA 510(k)

AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS

K-Number: K052290 · 2006-05-15

Decision Date2006-05-15
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Clearlab Pte , Ltd.. It received FDA 510(k) clearance on 2006-05-15 under 510(k) number K052290. 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 AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS?

AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS is a medical device that received FDA 510(k) clearance on 2006-05-15. The listed applicant is Clearlab Pte , Ltd.. The 510(k) number is K052290.

When did AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS receive FDA 510(k) clearance?

AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS received FDA 510(k) clearance on 2006-05-15, under 510(k) number K052290.

Who is the listed applicant for AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS?

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

What is the FDA product code for AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS?

The FDA product code for AQUASOFT ALL-DAY & ALL-DAY T (HIOXIFILCON A) DAILY WEAR CONTACT LENS is LPL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Clearlab Pte , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LPL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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