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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2017-10-20 under 510(k) 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. The listed applicant is CAO Group, Inc.. The 510(k) number is K171052.

When did Ultimate Contour, Ultimate Contour Mini receive FDA 510(k) clearance?

Ultimate Contour, Ultimate Contour Mini received FDA 510(k) clearance on 2017-10-20, under 510(k) number K171052.

Who is the listed applicant for Ultimate Contour, Ultimate Contour Mini?

The FDA 510(k) record lists CAO Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ultimate Contour, Ultimate Contour Mini?

The FDA product code for Ultimate Contour, Ultimate Contour Mini is PBX.

Other records listing CAO Group, Inc. as applicant

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Related Devices (Code: 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.

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