OPTICAL FRAMES AND SUNGLASSES
K-Number: K926564 · 1994-07-27
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Device Summary
Frequently Asked Questions
What is the OPTICAL FRAMES AND SUNGLASSES?
OPTICAL FRAMES AND SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-07-27. The listed applicant is Solstar Produktions GmbH. The 510(k) number is K926564.
When did OPTICAL FRAMES AND SUNGLASSES receive FDA 510(k) clearance?
OPTICAL FRAMES AND SUNGLASSES received FDA 510(k) clearance on 1994-07-27, under 510(k) number K926564.
Who is the listed applicant for OPTICAL FRAMES AND SUNGLASSES?
The FDA 510(k) record lists Solstar Produktions GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTICAL FRAMES AND SUNGLASSES?
The FDA product code for OPTICAL FRAMES AND SUNGLASSES 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 Solstar Produktions GmbH 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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