Pocketcpr

FDA 510(k) K112660 · Zoll Medical Corp

Substantially Equivalent

510(k) numberK112660

Submission

Device name
Pocketcpr
Applicant
Zoll Medical Corp
Pawtucket, RI, US
Received
September 13, 2011
Decision date
May 10, 2012
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LIX – Aid, Cardiopulmonary Resuscitation
Device class
Class II (moderate risk)
Regulation
21 CFR 870.5210
Specialty
Cardiovascular

CPR Aid device WITH feedback (visual, audio or both) on one or more CPR parameters (e.g., rate, depth, ventilation ratio, etc.), and contains software. Provides real-time feedback on CPR performance. Feedback can be audio, visual or both. Device contains software

Other 510(k)s with product code LIX

510(k)DeviceApplicantDecision
K201581CPR BandLIX · Traditional Credo03/06/2021SE
K183348Reusable Silicone Cover CPRmeter 2LIX · Special Laerdal Medical AS12/17/2018SE
K173886CPRmeter 2 CPR Feedback DeviceLIX · Traditional Laerdal Medical AS03/23/2018SE
K151702Reusable Full Silicone CoverLIX · Special Laerdal Medical AS08/13/2015SE
K123248CPR RSQ AssistLIX · Traditional Avantech, Inc.12/10/2013SE
K123597Truecpr Coaching DeviceLIX · Traditional Physio-Control, Inc.04/17/2013SE
K122050Cprmeter CPR Feedback DeviceLIX · Traditional Laerdal Medical A/S10/22/2012SE
K092408Rhythm of Life, Model R0901-05LIX · Traditional Rapid Response Solutions, LLC10/14/2009SE
K071321PocketcprLIX · Traditional Bio-Detek, Inc.09/12/2007SE
K010526Modification to the GripLIX · Traditional Elcare Innovations, Inc.12/13/2001SE

More from Elcare Innovations, Inc.

510(k)DeviceDecision
K233486731 Series VentilatorCBK · Traditional 12/13/2024SE
K202375ZOLL Propaq MMWI · Traditional 03/09/2021SE
K180482ZOLL Propaq MMHX · Traditional 11/30/2018SE
K172653Power InfuserFRN · Traditional 07/18/2018SE
K162832731 Series VentilatorsCBK · Traditional 08/02/2017SE
K170533Model 330 Multifunction AspiratorBTA · Traditional 04/18/2017SE
K142915ZOLL X SeriesMKJ · Traditional 12/03/2014SE
K141774Zoll X SeriesMKJ · Traditional 11/19/2014SE
K140502Zoll E Series AlsLDD · Traditional 11/06/2014SE
K133484Zoll X SeriesMKJ · Traditional 08/01/2014SE

Questions and answers

When was Pocketcpr cleared by the FDA?

Pocketcpr (K112660) received a 510(k) decision of Substantially Equivalent on May 10, 2012, 240 days after the submission was received.

What is the product code of K112660?

The FDA product code is LIX – Aid, Cardiopulmonary Resuscitation, a Class II (moderate risk) device regulated under 21 CFR 870.5210.