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FDA 510(k)

DATEMINDER CONTACT LENS CASE

K-Number: K945259 · 1995-01-24

Decision Date1995-01-24
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DATEMINDER CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Bruce A. Berkley. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K945259. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATEMINDER CONTACT LENS CASE?

DATEMINDER CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Bruce A. Berkley. The 510(k) number is K945259.

When did DATEMINDER CONTACT LENS CASE receive FDA 510(k) clearance?

DATEMINDER CONTACT LENS CASE received FDA 510(k) clearance on 1995-01-24, under 510(k) number K945259.

Who is the listed applicant for DATEMINDER CONTACT LENS CASE?

The FDA 510(k) record lists Bruce A. Berkley as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DATEMINDER CONTACT LENS CASE?

The FDA product code for DATEMINDER CONTACT LENS CASE is LRX.

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: LRX)

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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