YOLO CURVE
K-Number: K110342 · 2011-08-22
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Device Summary
Frequently Asked Questions
What is the YOLO CURVE?
YOLO CURVE is a medical device that received FDA 510(k) clearance on 2011-08-22. The listed applicant is Yolo Medical, Inc.. The 510(k) number is K110342.
When did YOLO CURVE receive FDA 510(k) clearance?
YOLO CURVE received FDA 510(k) clearance on 2011-08-22, under 510(k) number K110342.
Who is the listed applicant for YOLO CURVE?
The FDA 510(k) record lists Yolo Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YOLO CURVE?
The FDA product code for YOLO CURVE is ILY.
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 Yolo Medical, Inc. 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: ILY)
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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