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FDA 510(k)

POST MYDRIATIC SPECTACLES

K-Number: K904585 · 1990-10-26

Decision Date1990-10-26
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

POST MYDRIATIC SPECTACLES is the device name listed in this FDA 510(k) record. The listed applicant is Yorktowne Optical Co., Inc.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K904585. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POST MYDRIATIC SPECTACLES?

POST MYDRIATIC SPECTACLES is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Yorktowne Optical Co., Inc.. The 510(k) number is K904585.

When did POST MYDRIATIC SPECTACLES receive FDA 510(k) clearance?

POST MYDRIATIC SPECTACLES received FDA 510(k) clearance on 1990-10-26, under 510(k) number K904585.

Who is the listed applicant for POST MYDRIATIC SPECTACLES?

The FDA 510(k) record lists Yorktowne Optical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POST MYDRIATIC SPECTACLES?

The FDA product code for POST MYDRIATIC SPECTACLES is HQY.

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 Yorktowne Optical Co., Inc. 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.

Related Devices (Code: HQY)

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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