Atlas FDA

AUTOPULSE RESUSCITATION SYSTEM

FDA 510(k) clearance K022345 · decided 2002-08-15

Clearance details

K-number
K022345
Device name
AUTOPULSE RESUSCITATION SYSTEM
Applicant
Revivant Corp.
Decision
Substantially Equivalent
Date received
2002-07-19
Decision date
2002-08-15
Days to decision
27 days
Clearance type
Special
Product code
DRM
Device class
2
Regulation number
870.5200
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Sunnyvale, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
AutoPulse NXT Resuscitation System (K221700)Zoll Circulation, Inc.2023-03-09
RMU-2000 Automated Chest Compression System (K211289)Defibtech, LLC2021-11-09
LUCAS 3 Chest Compression System (K173553)Jolife AB2018-02-08
LUCAS 3 Chest Compression System (K161768)Jolife AB2016-11-09
ROSC-U Mini Chest Compressor (RMCC) (K153628)Resuscitation International, LLC2016-01-30
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM (K141809)Defibtech, LLC2014-10-27
AUTOPULSE RESUSCITATION SYSTEM MODEL 1000 (K112998)Zoll Circulation2012-03-15
MINIATURIZE CHEST COMPRESSOR (MCC) (K102068)Resuscitation International2010-11-16
LUCAS 2 (K090422)Jolife AB2009-06-17
AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 (K072527)Zoll Circulation2008-03-19
THUMPER, MODEL: 1008 (K073079)Michigan Instruments, Inc.2008-02-14
AUTOPULSE RESUSCITATION SYSTEM MODEL100 (K063602)Zoll Circulation2006-12-21

Recalls involving this device

RecordFirmDate
Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery recall (Z-2090-2014)Zoll Circulation, Inc.2014-07-22
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoP recall (Z-0658-2013)Zoll Circulation, Inc.2013-01-09