Ultimate Contour, Ultimate Contour Mini
K-Number: K171052 · 2017-10-20
ApplicantCAO Group, Inc.
Decision Date2017-10-20
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Ultimate Contour, Ultimate Contour Mini is a medical device manufactured by CAO Group, Inc.. It received FDA 510(k) clearance on 2017-10-20 under approval number K171052. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ultimate Contour, Ultimate Contour Mini?
Ultimate Contour, Ultimate Contour Mini is a medical device that received FDA 510(k) clearance on 2017-10-20. It is manufactured by CAO Group, Inc.. The 510(k) number is K171052.
When was Ultimate Contour, Ultimate Contour Mini approved by the FDA?
Ultimate Contour, Ultimate Contour Mini received FDA 510(k) clearance on 2017-10-20, under approval number K171052.
What company makes Ultimate Contour, Ultimate Contour Mini?
Ultimate Contour, Ultimate Contour Mini is manufactured by CAO Group, Inc..
What is the FDA product code for Ultimate Contour, Ultimate Contour Mini?
The FDA product code for Ultimate Contour, Ultimate Contour Mini is PBX.
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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.