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FDA 510(k)

AD7 PLASTIC MULTIFOCAL EYEGLASS LENS

K-Number: K761163 · 1976-12-16

Decision Date1976-12-16
Product CodeHQG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AD7 PLASTIC MULTIFOCAL EYEGLASS LENS is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761163. The device is classified under product code HQG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AD7 PLASTIC MULTIFOCAL EYEGLASS LENS?

AD7 PLASTIC MULTIFOCAL EYEGLASS LENS is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is American Optical Corp.. The 510(k) number is K761163.

When did AD7 PLASTIC MULTIFOCAL EYEGLASS LENS receive FDA 510(k) clearance?

AD7 PLASTIC MULTIFOCAL EYEGLASS LENS received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761163.

Who is the listed applicant for AD7 PLASTIC MULTIFOCAL EYEGLASS LENS?

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

What is the FDA product code for AD7 PLASTIC MULTIFOCAL EYEGLASS LENS?

The FDA product code for AD7 PLASTIC MULTIFOCAL EYEGLASS LENS is HQG.

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.

Other records listing American Optical Corp. as applicant

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.

View all 35 devices →

Related Devices (Code: HQG)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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