FDA 510(k)

AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION

K-Number: K022687 · 2002-11-19

Decision Date2002-11-19

Product CodeLYL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Ciba Vision Corporation. It received FDA 510(k) clearance on 2002-11-19 under 510(k) number K022687. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION?

AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION is a medical device that received FDA 510(k) clearance on 2002-11-19. The listed applicant is Ciba Vision Corporation. The 510(k) number is K022687.

When did AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION receive FDA 510(k) clearance?

AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION received FDA 510(k) clearance on 2002-11-19, under 510(k) number K022687.

Who is the listed applicant for AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION?

The FDA 510(k) record lists Ciba Vision Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION?

The FDA product code for AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION is LYL.

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Related Devices (Code: LYL)

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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.