FDA 510(k) Applications for Medical Device Product Code "DRM"
(Compressor, Cardiac, External)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K141809 | DEFIBTECH, LLC | RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM | 10/27/2014 |
| K211289 | Defibtech, LLC | RMU-2000 Automated Chest Compression System | 11/09/2021 |
| K024215 | ENERTRON ENGINEERING CO. | ENERTRON CPR JACK | 05/14/2004 |
| K053403 | JOLIFE AB | LUCAS | 02/01/2006 |
| K090422 | JOLIFE AB | LUCAS 2 | 06/17/2009 |
| K173553 | Jolife AB | LUCAS 3 Chest Compression System | 02/08/2018 |
| K161768 | Jolife AB | LUCAS 3 Chest Compression System | 11/09/2016 |
| K062401 | JOLIFE AB | MODIFICATION TO LUCAS | 09/28/2006 |
| K062119 | MEDICAL PRODUCTS MFG., LLC | HLR MODEL 601 HEART LUNG RESUSCITATOR AND HEARTSAVER 100 | 09/22/2006 |
| K972525 | MICHIGAN INSTRUMENTS, INC. | THUMPER | 10/02/1997 |
| K962237 | MICHIGAN INSTRUMENTS, INC. | THUMPER CARDIOPULMONARY RESUSCITATOR | 09/05/1996 |
| K073079 | MICHIGAN INSTRUMENTS, INC. | THUMPER, MODEL: 1008 | 02/14/2008 |
| K102068 | RESUSCITATION INTERNATIONAL | MINIATURIZE CHEST COMPRESSOR (MCC) | 11/16/2010 |
| K153628 | Resuscitation International, LLC | ROSC-U Mini Chest Compressor (RMCC) | 01/30/2016 |
| K022345 | REVIVANT CORP. | AUTOPULSE RESUSCITATION SYSTEM | 08/15/2002 |
| K040453 | REVIVANT CORP. | AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 | 03/11/2004 |
| K011046 | REVIVANT CORP. | AUTOPULSE, MODEL 100 | 10/25/2001 |
| K032852 | REVIVANT CORP. | MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100 | 11/12/2003 |
| K063602 | ZOLL CIRCULATION | AUTOPULSE RESUSCITATION SYSTEM MODEL100 | 12/21/2006 |
| K112998 | ZOLL CIRCULATION | AUTOPULSE RESUSCITATION SYSTEM MODEL 1000 | 03/15/2012 |
| K072527 | ZOLL CIRCULATION | AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 | 03/19/2008 |
| K221700 | ZOLL Circulation, Inc. | AutoPulse NXT Resuscitation System | 03/09/2023 |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact
