Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION

K-Number: K994021 · 2000-02-22

Decision Date2000-02-22
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Strieter Clinical Research Laboratories, Inc.. It received FDA 510(k) clearance on 2000-02-22 under 510(k) number K994021. 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 CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION?

CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION is a medical device that received FDA 510(k) clearance on 2000-02-22. The listed applicant is Strieter Clinical Research Laboratories, Inc.. The 510(k) number is K994021.

When did CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION receive FDA 510(k) clearance?

CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION received FDA 510(k) clearance on 2000-02-22, under 510(k) number K994021.

Who is the listed applicant for CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION?

The FDA 510(k) record lists Strieter Clinical Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION?

The FDA product code for CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION is LYL.

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.

Related Devices (Code: LYL)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑