Cleared Traditional

K151689 - MetaNeb 4 System
(FDA 510(k) Clearance)

Mar 2016
Decision
268d
Days
Class 2
Risk

K151689 is an FDA 510(k) clearance for the MetaNeb 4 System. This device is classified as a Device, Positive Pressure Breathing, Intermittent (Class II - Special Controls, product code NHJ).

Submitted by Hill-Rom Services Pte, Ltd. (Singapore, SG). The FDA issued a Cleared decision on March 17, 2016, 268 days after receiving the submission on June 23, 2015.

This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5905.

Submission Details

510(k) Number K151689 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 2015
Decision Date March 17, 2016
Days to Decision 268 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF

Device Classification

Product Code NHJ — Device, Positive Pressure Breathing, Intermittent
Device Class Class II - Special Controls
CFR Regulation 21 CFR 868.5905