FDA 510(k)

Quickie(r) Q700-UP M

K-Number: K172384 · 2018-01-16

Decision Date2018-01-16

Product CodeIPL

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Quickie(r) Q700-UP M is a medical device manufactured by Sunrise Medical (Us), LLC. It received FDA 510(k) clearance on 2018-01-16 under approval number K172384. 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 Quickie(r) Q700-UP M?

Quickie(r) Q700-UP M is a medical device that received FDA 510(k) clearance on 2018-01-16. It is manufactured by Sunrise Medical (Us), LLC. The 510(k) number is K172384.

When was Quickie(r) Q700-UP M approved by the FDA?

Quickie(r) Q700-UP M received FDA 510(k) clearance on 2018-01-16, under approval number K172384.

What company makes Quickie(r) Q700-UP M?

Quickie(r) Q700-UP M is manufactured by Sunrise Medical (Us), LLC.

What is the FDA product code for Quickie(r) Q700-UP M?

The FDA product code for Quickie(r) Q700-UP M is IPL.

Other Devices by Sunrise Medical (Us), LLC

K160031Quickie Pulse (Models 6BC, 6SC, 6CC, 5BC, 5CC, 6MPC) and Zippie ZM-310 (Models BC, SC) K220213Empulse R90

Related Devices (Code: IPL)

K163451Action Trackstander models TR1816, TR1820, TR2016, and TR2020Action Manufacturing, Inc. K191874F5 Corpus VSPermobil AB K182257UPnRIDEUpnride Robotics , Ltd. K191376Modular Power Standing SystemMotion Concepts K191334Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08Matia Robotics (Us), Inc. K190682Explorer MiniPermobil AB

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.