SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION
K-Number: K974485 · 1998-02-24
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Device Summary
Frequently Asked Questions
What is the SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION?
SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION is a medical device that received FDA 510(k) clearance on 1998-02-24. The listed applicant is Szabocsik and Assoc.. The 510(k) number is K974485.
When did SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION receive FDA 510(k) clearance?
SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION received FDA 510(k) clearance on 1998-02-24, under 510(k) number K974485.
Who is the listed applicant for SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION?
The FDA 510(k) record lists Szabocsik and Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION?
The FDA product code for SAUFLON ALL-IN-ONE LIGHT CONTACT LENS SOLUTION is LPN.
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 Szabocsik and Assoc. 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: LPN)
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.
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