Cleared Traditional

K133859 - WATCH-PAT200U (WP200U)
(FDA 510(k) Clearance)

May 2014
Decision
162d
Days
Class 2
Risk

K133859 is an FDA 510(k) clearance for the WATCH-PAT200U (WP200U). This device is classified as a Ventilatory Effort Recorder (Class II - Special Controls, product code MNR).

Submitted by Itamar Medical , Ltd. (Washington, US). The FDA issued a Cleared decision on May 30, 2014, 162 days after receiving the submission on December 19, 2013.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.2375.

Submission Details

510(k) Number K133859 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 19, 2013
Decision Date May 30, 2014
Days to Decision 162 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code MNR — Ventilatory Effort Recorder
Device Class Class II - Special Controls
CFR Regulation 21 CFR 868.2375