SILHOUETTE, SUNLIMETED,ADIDAS
K-Number: K944160 · 1994-09-28
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Device Summary
Frequently Asked Questions
What is the SILHOUETTE, SUNLIMETED,ADIDAS?
SILHOUETTE, SUNLIMETED,ADIDAS is a medical device that received FDA 510(k) clearance on 1994-09-28. The listed applicant is Silhouette Optical , Ltd.. The 510(k) number is K944160.
When did SILHOUETTE, SUNLIMETED,ADIDAS receive FDA 510(k) clearance?
SILHOUETTE, SUNLIMETED,ADIDAS received FDA 510(k) clearance on 1994-09-28, under 510(k) number K944160.
Who is the listed applicant for SILHOUETTE, SUNLIMETED,ADIDAS?
The FDA 510(k) record lists Silhouette Optical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SILHOUETTE, SUNLIMETED,ADIDAS?
The FDA product code for SILHOUETTE, SUNLIMETED,ADIDAS is HQZ.
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 Silhouette Optical , Ltd. 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: HQZ)
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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