510(k) K140707

LIFEBORNE INFANT RESUSCITATOR by International Biomedical — Product Code BTL

K140707 is an FDA 510(k) premarket notification submitted by International Biomedical for the device "LIFEBORNE INFANT RESUSCITATOR". The FDA issued a decision of Substantially Equivalent on May 28, 2014. The device falls under product code BTL (Ventilator, Emergency, Powered (Resuscitator)), a Class II device regulated under 21 CFR 868.5925. International Biomedical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 28, 2014
Date Received
March 20, 2014
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Emergency, Powered (Resuscitator)
Device Class
Class II
Regulation Number
868.5925
Review Panel
AN
Submission Type