O-Two E700,O-TWO E600,O-TWO E500
FDA 510(k) K141595 · O-Two Medical Technologies, Inc.
510(k) numberK141595
Submission
- Device name
- O-Two E700,O-TWO E600,O-TWO E500
- Applicant
- O-Two Medical Technologies, Inc.
Mississauga, CA - Received
- June 13, 2014
- Decision date
- March 16, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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
Other 510(k)s with product code BTL
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K242769 | VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)BTL · Traditional | Draegerwerk AG & CO Kgaa | 04/04/2025SE |
| K221634 | Oxymag - Transport and Emergency VentilatorBTL · Traditional | Magnamed Tecnologia Medica S/A | 05/24/2023SE |
| K202219 | VORTRAN GO2VENT with PEEP ValveBTL · Traditional | Vortran Medical Technology 1, Inc. | 02/11/2021SE |
| K193191 | MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagBTL · Traditional | Weinmann Emergency Medical Technology GmbH + Co.… | 11/20/2020SE |
| K182956 | Puffin Lite Infant Resuscitation SystemBTL · Special | International Biomedical | 01/18/2019SE |
| K173373 | SafeT T-Piece ResuscitatorBTL · Traditional | Ventlab, LLC | 11/16/2018SE |
| K161420 | Moves SLCBTL · Traditional | Thornhill Research, Inc. | 06/06/2017SE |
| K162968 | Vortran GO2VENTBTL · Traditional | Vortran Medical Technology 1, Inc. | 04/10/2017SE |
| K142096 | T-Piece ResuscitatorBTL · Traditional | Mercury Medical | 10/17/2014SE |
| K140049 | Moves SLCBTL · Traditional | Thornhill Research, Inc. | 05/29/2014SE |
More from Thornhill Research, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K173205 | Equinox AdvantageBZR · Traditional | 08/29/2018SE |
| K113687 | Equinox RelieveBZR · Traditional | 04/30/2012SE |
| K112546 | O_Two CPAP SystemBYE · Traditional | 12/27/2011SE |
| K093862 | Carevent Handheld CPAP SystemBTL · Traditional | 05/06/2010SE |
| K081330 | Carevent Par (Public Access Resuscitator)BTL · Traditional | 03/06/2009SE |
| K051469 | Carevent Atv+ and Carevent MRIBTL · Traditional | 09/28/2005SE |
| K051889 | Carevent Ca and DraBTL · Special | 08/30/2005SE |
Questions and answers
When was O-Two E700,O-TWO E600,O-TWO E500 cleared by the FDA?
O-Two E700,O-TWO E600,O-TWO E500 (K141595) received a 510(k) decision of Substantially Equivalent on March 16, 2015, 276 days after the submission was received.
What is the product code of K141595?
The FDA product code is BTL – Ventilator, Emergency, Powered (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5925.