510(k) K151120

Simple T Pediatric Nasal Mask by Respironics, Inc. — Product Code BZD

K151120 is an FDA 510(k) premarket notification submitted by Respironics, Inc. for the device "Simple T Pediatric Nasal Mask". The FDA issued a decision of Substantially Equivalent on April 15, 2016. The device falls under product code BZD (Ventilator, Non-Continuous (Respirator)), a Class II device regulated under 21 CFR 868.5905. Respironics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 15, 2016
Date Received
April 27, 2015
Clearance Type
Abbreviated
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Non-Continuous (Respirator)
Device Class
Class II
Regulation Number
868.5905
Review Panel
AN
Submission Type