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FDA 510(k)

THE CONTACT LENS ASSIST BRUSH

K-Number: K864502 · 1987-01-20

Decision Date1987-01-20
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE CONTACT LENS ASSIST BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Young and Moore Enterprises, Inc.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K864502. 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 THE CONTACT LENS ASSIST BRUSH?

THE CONTACT LENS ASSIST BRUSH is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Young and Moore Enterprises, Inc.. The 510(k) number is K864502.

When did THE CONTACT LENS ASSIST BRUSH receive FDA 510(k) clearance?

THE CONTACT LENS ASSIST BRUSH received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864502.

Who is the listed applicant for THE CONTACT LENS ASSIST BRUSH?

The FDA 510(k) record lists Young and Moore Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE CONTACT LENS ASSIST BRUSH?

The FDA product code for THE CONTACT LENS ASSIST BRUSH 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.

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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