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FDA 510(k)

THE ALBERTA LENS SM2, SULFOCON B

K-Number: K010454 · 2001-08-01

Decision Date2001-08-01
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE ALBERTA LENS SM2, SULFOCON B is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Optical Research , Ltd.. It received FDA 510(k) clearance on 2001-08-01 under 510(k) number K010454. 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 THE ALBERTA LENS SM2, SULFOCON B?

THE ALBERTA LENS SM2, SULFOCON B is a medical device that received FDA 510(k) clearance on 2001-08-01. The listed applicant is Progressive Optical Research , Ltd.. The 510(k) number is K010454.

When did THE ALBERTA LENS SM2, SULFOCON B receive FDA 510(k) clearance?

THE ALBERTA LENS SM2, SULFOCON B received FDA 510(k) clearance on 2001-08-01, under 510(k) number K010454.

Who is the listed applicant for THE ALBERTA LENS SM2, SULFOCON B?

The FDA 510(k) record lists Progressive Optical Research , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE ALBERTA LENS SM2, SULFOCON B?

The FDA product code for THE ALBERTA LENS SM2, SULFOCON B 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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