CUDA PRODUCTS CORP. LIGHTSOURCES
K-Number: K933369 · 1994-01-03
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Device Summary
Frequently Asked Questions
What is the CUDA PRODUCTS CORP. LIGHTSOURCES?
CUDA PRODUCTS CORP. LIGHTSOURCES is a medical device that received FDA 510(k) clearance on 1994-01-03. The listed applicant is Cuda Products Co.. The 510(k) number is K933369.
When did CUDA PRODUCTS CORP. LIGHTSOURCES receive FDA 510(k) clearance?
CUDA PRODUCTS CORP. LIGHTSOURCES received FDA 510(k) clearance on 1994-01-03, under 510(k) number K933369.
Who is the listed applicant for CUDA PRODUCTS CORP. LIGHTSOURCES?
The FDA 510(k) record lists Cuda Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUDA PRODUCTS CORP. LIGHTSOURCES?
The FDA product code for CUDA PRODUCTS CORP. LIGHTSOURCES is FCW.
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 Cuda Products Co. 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: FCW)
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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