CR-39 PLASTIC LENSES FOR EYEGLASSES
K-Number: K882308 · 1988-07-22
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Device Summary
Frequently Asked Questions
What is the CR-39 PLASTIC LENSES FOR EYEGLASSES?
CR-39 PLASTIC LENSES FOR EYEGLASSES is a medical device that received FDA 510(k) clearance on 1988-07-22. The listed applicant is Automated Lens System. The 510(k) number is K882308.
When did CR-39 PLASTIC LENSES FOR EYEGLASSES receive FDA 510(k) clearance?
CR-39 PLASTIC LENSES FOR EYEGLASSES received FDA 510(k) clearance on 1988-07-22, under 510(k) number K882308.
Who is the listed applicant for CR-39 PLASTIC LENSES FOR EYEGLASSES?
The FDA 510(k) record lists Automated Lens System as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CR-39 PLASTIC LENSES FOR EYEGLASSES?
The FDA product code for CR-39 PLASTIC LENSES FOR EYEGLASSES 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.
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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