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FDA 510(k)

JSZ MULTIACTION GP CONTACT LENS SOLUTION

K-Number: K060924 · 2006-06-28

Decision Date2006-06-28
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

JSZ MULTIACTION GP CONTACT LENS SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Szabocsik and Associates. It received FDA 510(k) clearance on 2006-06-28 under 510(k) number K060924. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JSZ MULTIACTION GP CONTACT LENS SOLUTION?

JSZ MULTIACTION GP CONTACT LENS SOLUTION is a medical device that received FDA 510(k) clearance on 2006-06-28. The listed applicant is Szabocsik and Associates. The 510(k) number is K060924.

When did JSZ MULTIACTION GP CONTACT LENS SOLUTION receive FDA 510(k) clearance?

JSZ MULTIACTION GP CONTACT LENS SOLUTION received FDA 510(k) clearance on 2006-06-28, under 510(k) number K060924.

Who is the listed applicant for JSZ MULTIACTION GP CONTACT LENS SOLUTION?

The FDA 510(k) record lists Szabocsik and Associates as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JSZ MULTIACTION GP CONTACT LENS SOLUTION?

The FDA product code for JSZ MULTIACTION GP 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 Associates 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

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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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