AR DIACOAT SINGLE VISION LENSES
K-Number: K873245 · 1987-10-05
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Device Summary
Frequently Asked Questions
What is the AR DIACOAT SINGLE VISION LENSES?
AR DIACOAT SINGLE VISION LENSES is a medical device that received FDA 510(k) clearance on 1987-10-05. The listed applicant is Seiko Optical Products of America, Inc.. The 510(k) number is K873245.
When did AR DIACOAT SINGLE VISION LENSES receive FDA 510(k) clearance?
AR DIACOAT SINGLE VISION LENSES received FDA 510(k) clearance on 1987-10-05, under 510(k) number K873245.
Who is the listed applicant for AR DIACOAT SINGLE VISION LENSES?
The FDA 510(k) record lists Seiko Optical Products of America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AR DIACOAT SINGLE VISION LENSES?
The FDA product code for AR DIACOAT SINGLE VISION LENSES 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 Seiko Optical Products of America, 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: 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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