Cardiopulmunary Resuscitator
FDA 510(k) K811909 · Michigan Instruments, Inc.
510(k) numberK811909
Submission
- Device name
- Cardiopulmunary Resuscitator
- Applicant
- Michigan Instruments, Inc.
Mchenry, IL, US - Received
- July 1, 1981
- Decision date
- July 16, 1981
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- DRM – Compressor, Cardiac, External
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.5200
- Specialty
- Cardiovascular
Other 510(k)s with product code DRM
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K221700 | AutoPulse NXT Resuscitation SystemDRM · Traditional | Zoll Circulation, Inc. | 03/09/2023SE |
| K211289 | RMU-2000 Automated Chest Compression SystemDRM · Traditional | Defibtech, LLC | 11/09/2021SE |
| K173553 | LUCAS 3 Chest Compression SystemDRM · Traditional | Jolife AB | 02/08/2018SE |
| K161768 | LUCAS 3 Chest Compression SystemDRM · Traditional | Jolife AB | 11/09/2016SE |
| K153628 | ROSC-U Mini Chest Compressor (RMCC)DRM · Traditional | Resuscitation International, LLC | 01/30/2016SE |
| K141809 | RMU-1000 Automated Chest Compression SystemDRM · Traditional | Defibtech, LLC | 10/27/2014SE |
| K112998 | Autopulse Resuscitation System Model 1000DRM · Traditional | Zoll Circulation | 03/15/2012SE |
| K102068 | Miniaturize Chest Compressor (MCC)DRM · Traditional | Resuscitation International | 11/16/2010SE |
| K090422 | Lucas 2DRM · Traditional | Jolife AB | 06/17/2009SE |
| K072527 | Autopulse Resuscitation System, Model 100DRM · Traditional | Zoll Circulation | 03/19/2008SE |
More from Zoll Circulation
| 510(k) | Device | Decision |
|---|---|---|
| K073079 | Thumper, Model: 1008DRM · Traditional | 02/14/2008SE |
| K972525 | ThumperDRM · Traditional | 10/02/1997SE |
| K962237 | Thumper Cardiopulmonary ResuscitatorDRM · Traditional | 09/05/1996SE |
| K895954 | Laryngostat Laryngoscope HandleCCW · Traditional | 10/30/1989SE |
| K851139 | Thumper Cardiopulmonary Resuscitator 1005DRM · Traditional | 05/15/1985SE |
| K833879 | Cardiopulmonary ResuscitatorDRM · Traditional | 12/27/1983SE |
Questions and answers
When was Cardiopulmunary Resuscitator cleared by the FDA?
Cardiopulmunary Resuscitator (K811909) received a 510(k) decision of Substantially Equivalent on July 16, 1981, 15 days after the submission was received.
What is the product code of K811909?
The FDA product code is DRM – Compressor, Cardiac, External, a Class II (moderate risk) device regulated under 21 CFR 870.5200.