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FDA 510(k)

CONTACT LENS STORAGE CASE

K-Number: K030987 · 2003-06-12

Decision Date2003-06-12
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTACT LENS STORAGE CASE is the device name listed in this FDA 510(k) record. The listed applicant is Pelican Products. It received FDA 510(k) clearance on 2003-06-12 under 510(k) number K030987. 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 CONTACT LENS STORAGE CASE?

CONTACT LENS STORAGE CASE is a medical device that received FDA 510(k) clearance on 2003-06-12. The listed applicant is Pelican Products. The 510(k) number is K030987.

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

CONTACT LENS STORAGE CASE received FDA 510(k) clearance on 2003-06-12, under 510(k) number K030987.

Who is the listed applicant for CONTACT LENS STORAGE CASE?

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

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

The FDA product code for CONTACT LENS STORAGE 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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