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FDA 510(k)

OXYCON LENS

K-Number: K990895 · 1999-04-14

Decision Date1999-04-14
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OXYCON LENS is the device name listed in this FDA 510(k) record. The listed applicant is Concise Contact Lens Co.. It received FDA 510(k) clearance on 1999-04-14 under 510(k) number K990895. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYCON LENS?

OXYCON LENS is a medical device that received FDA 510(k) clearance on 1999-04-14. The listed applicant is Concise Contact Lens Co.. The 510(k) number is K990895.

When did OXYCON LENS receive FDA 510(k) clearance?

OXYCON LENS received FDA 510(k) clearance on 1999-04-14, under 510(k) number K990895.

Who is the listed applicant for OXYCON LENS?

The FDA 510(k) record lists Concise Contact Lens Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYCON LENS?

The FDA product code for OXYCON LENS is HQD.

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: HQD)

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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