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FDA 510(k)

NUPRO MODEL 13016901

K-Number: K103160 · 2011-01-06

ApplicantCAO Group, Inc.
Decision Date2011-01-06
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NUPRO MODEL 13016901 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 2011-01-06 under 510(k) number K103160. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NUPRO MODEL 13016901?

NUPRO MODEL 13016901 is a medical device that received FDA 510(k) clearance on 2011-01-06. The listed applicant is CAO Group, Inc.. The 510(k) number is K103160.

When did NUPRO MODEL 13016901 receive FDA 510(k) clearance?

NUPRO MODEL 13016901 received FDA 510(k) clearance on 2011-01-06, under 510(k) number K103160.

Who is the listed applicant for NUPRO MODEL 13016901?

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 NUPRO MODEL 13016901?

The FDA product code for NUPRO MODEL 13016901 is LBH.

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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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