CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION
K-Number: K994021 · 2000-02-22
Advertisement
Device Summary
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.
Advertisement