POST MYDRIATIC SPECTACLES
K-Number: K904585 · 1990-10-26
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Device Summary
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
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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