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FDA 510(k)

UPnRIDE

K-Number: K182257 · 2019-09-12

ApplicantUpnride Robotics , Ltd.
Decision Date2019-09-12
Product CodeIPL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

UPnRIDE is the device name listed in this FDA 510(k) record. The listed applicant is Upnride Robotics , Ltd.. It received FDA 510(k) clearance on 2019-09-12 under 510(k) number K182257. The device is classified under product code IPL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UPnRIDE?

UPnRIDE is a medical device that received FDA 510(k) clearance on 2019-09-12. The listed applicant is Upnride Robotics , Ltd.. The 510(k) number is K182257.

When did UPnRIDE receive FDA 510(k) clearance?

UPnRIDE received FDA 510(k) clearance on 2019-09-12, under 510(k) number K182257.

Who is the listed applicant for UPnRIDE?

The FDA 510(k) record lists Upnride Robotics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UPnRIDE?

The FDA product code for UPnRIDE is IPL.

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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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