Cleared Traditional

K153070 - Watch-PAT200U
(FDA 510(k) Clearance)

Jul 2016
Decision
278d
Days
Class 2
Risk

K153070 is an FDA 510(k) clearance for the Watch-PAT200U. This device is classified as a Ventilatory Effort Recorder (Class II - Special Controls, product code MNR).

Submitted by Itamar Medical , Ltd. (Caesarea, IL). The FDA issued a Cleared decision on July 26, 2016, 278 days after receiving the submission on October 22, 2015.

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

Submission Details

510(k) Number K153070 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 22, 2015
Decision Date July 26, 2016
Days to Decision 278 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