510(k) K110471

BABI PLUS INFANT NASAL CANNULA SYSTEM by A Plus Medical — Product Code BZD

K110471 is an FDA 510(k) premarket notification submitted by A Plus Medical for the device "BABI PLUS INFANT NASAL CANNULA SYSTEM". The FDA issued a decision of Substantially Equivalent on October 7, 2011. The device falls under product code BZD (Ventilator, Non-Continuous (Respirator)), a Class II device regulated under 21 CFR 868.5905. A Plus Medical has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 7, 2011
Date Received
February 18, 2011
Clearance Type
Special
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