WATCH-PAT200U (WP200U)

FDA 510(k) K133859 · Itamar Medical , Ltd.

Substantially Equivalent

510(k) numberK133859

Submission

Device name
WATCH-PAT200U (WP200U)
Applicant
Itamar Medical , Ltd.
Washington, DC, US
Received
December 19, 2013
Decision date
May 30, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNR – Ventilatory Effort Recorder
Device class
Class II (moderate risk)
Regulation
21 CFR 868.2375
Specialty
Anesthesiology

Other 510(k)s with product code MNR

510(k)DeviceApplicantDecision
K254042WatchPAT SWMNR · Traditional Itamar Medical , Ltd.07/31/2026SE
K260050WRAP SystemMNR · Traditional Huneo, LLC07/15/2026SE
K253148RX-1 SleepMNR · Traditional Vivaquant, Inc. Dba Rhythm Express06/22/2026SE
K252628CassieMNR · Traditional Wesper, Inc.04/27/2026SE
K252497Sansa HsatMNR · Traditional Huxley Medical12/10/2025SE
K250882Sansa HsatMNR · Traditional Huxley Medical10/29/2025SE
K250460WatchPAT400 (WP400)MNR · Traditional Itamar Medical , Ltd.09/05/2025SE
K252383Somfit DMNR · Special Compumedics Limited08/28/2025SE
K243220Onera STS 2 (ONERA STS 2)MNR · Traditional Onera B.V.07/03/2025SE
K242224Happy Health Home Sleep TestMNR · Traditional Happy Health, Inc.06/18/2025SE

More from Happy Health, Inc.

510(k)DeviceDecision
K254042WatchPAT SWMNR · Traditional 07/31/2026SE
K250460WatchPAT400 (WP400)MNR · Traditional 09/05/2025SE
K223675WatchPAT ONE (WP1)MNR · Special 01/06/2023SE
K211557EndoPATxDQK · Traditional 12/29/2022SE
K222331WatchPAT300 (WP300)MNR · Special 09/14/2022SE
K203839WatchPAT200U (WP200U)MNR · Traditional 03/21/2022SE
K183559WatchPAT ONEMNR · Traditional 06/05/2019SE
K180775Watch-PAT300MNR · Traditional 08/17/2018SE
K161579Watch-PAT200UMNR · Traditional 02/24/2017SE
K153070Watch-PAT200UMNR · Traditional 07/26/2016SE

Questions and answers

When was WATCH-PAT200U (WP200U) cleared by the FDA?

WATCH-PAT200U (WP200U) (K133859) received a 510(k) decision of Substantially Equivalent on May 30, 2014, 162 days after the submission was received.

What is the product code of K133859?

The FDA product code is MNR – Ventilatory Effort Recorder, a Class II (moderate risk) device regulated under 21 CFR 868.2375.