CURA COMPENSATOR
K-Number: K131150 · 2013-07-30
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Device Summary
Frequently Asked Questions
What is the CURA COMPENSATOR?
CURA COMPENSATOR is a medical device that received FDA 510(k) clearance on 2013-07-30. The listed applicant is Cura Medical Technologies, LLC. The 510(k) number is K131150.
When did CURA COMPENSATOR receive FDA 510(k) clearance?
CURA COMPENSATOR received FDA 510(k) clearance on 2013-07-30, under 510(k) number K131150.
Who is the listed applicant for CURA COMPENSATOR?
The FDA 510(k) record lists Cura Medical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CURA COMPENSATOR?
The FDA product code for CURA COMPENSATOR is IXI.
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 Cura Medical Technologies, LLC 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: IXI)
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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