Lifeborne Infant Resuscitator

FDA 510(k) K140707 · International Biomedical

Substantially Equivalent

510(k) numberK140707

Submission

Device name
Lifeborne Infant Resuscitator
Applicant
International Biomedical
Austin, TX, US
Received
March 20, 2014
Decision date
May 28, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
BTL – Ventilator, Emergency, Powered (Resuscitator)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5925
Specialty
Anesthesiology
Life-sustaining
Yes

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K202219VORTRAN GO2VENT with PEEP ValveBTL · Traditional Vortran Medical Technology 1, Inc.02/11/2021SE
K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagBTL · Traditional Weinmann Emergency Medical Technology GmbH + Co.…11/20/2020SE
K182956Puffin Lite Infant Resuscitation SystemBTL · Special International Biomedical01/18/2019SE
K173373SafeT T-Piece ResuscitatorBTL · Traditional Ventlab, LLC11/16/2018SE
K161420Moves SLCBTL · Traditional Thornhill Research, Inc.06/06/2017SE
K162968Vortran GO2VENTBTL · Traditional Vortran Medical Technology 1, Inc.04/10/2017SE
K141595O-Two E700,O-TWO E600,O-TWO E500BTL · Traditional O-Two Medical Technologies, Inc.03/16/2015SE
K142096T-Piece ResuscitatorBTL · Traditional Mercury Medical10/17/2014SE

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Questions and answers

When was Lifeborne Infant Resuscitator cleared by the FDA?

Lifeborne Infant Resuscitator (K140707) received a 510(k) decision of Substantially Equivalent on May 28, 2014, 69 days after the submission was received.

What is the product code of K140707?

The FDA product code is BTL – Ventilator, Emergency, Powered (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5925.