SOLSTAR BRILLENMODE SUNGLASSES
K-Number: K930562 · 1993-08-17
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Device Summary
Frequently Asked Questions
What is the SOLSTAR BRILLENMODE SUNGLASSES?
SOLSTAR BRILLENMODE SUNGLASSES is a medical device that received FDA 510(k) clearance on 1993-08-17. The listed applicant is Solstar Produktions GmbH. The 510(k) number is K930562.
When did SOLSTAR BRILLENMODE SUNGLASSES receive FDA 510(k) clearance?
SOLSTAR BRILLENMODE SUNGLASSES received FDA 510(k) clearance on 1993-08-17, under 510(k) number K930562.
Who is the listed applicant for SOLSTAR BRILLENMODE 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 SOLSTAR BRILLENMODE SUNGLASSES?
The FDA product code for SOLSTAR BRILLENMODE 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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