Evita V800, Evita V600
FDA 510(k) K222024 · Draegerwerk AG & CO Kgaa
510(k) numberK222024
Submission
- Device name
- Evita V800, Evita V600
- Applicant
- Draegerwerk AG & CO Kgaa
Luebeck, DE - Received
- July 11, 2022
- Decision date
- May 16, 2023
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- CBK – Ventilator, Continuous, Facility Use
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5895
- Specialty
- Anesthesiology
- Life-sustaining
- Yes
Other 510(k)s with product code CBK
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253647 | Evita (V800); Evita (V600)CBK · Traditional | Draegerwerk AG & CO Kgaa | 05/07/2026SE |
| K252663 | Inbentus VersatileCBK · Traditional | Iconic Solutions by Murcia, SL | 04/14/2026SE |
| K251888 | VPAP Pediatric Face MaskCBK · Traditional | Hsiner Co., Ltd. | 03/12/2026SE |
| K232365 | Vivo 45 LSCBK · Traditional | Oconnell Regulatory Consultants, Inc. | 12/19/2025SE |
| K252173 | F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits Size A…CBK · Traditional | Fisher & Paykel Healthcare, Ltd. | 09/10/2025SE |
| K243767 | SV600, SV800 VentilatorCBK · Traditional | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. | 08/28/2025SE |
| K251133 | AVEA disposable expiratory filter/water trap (11790)CBK · Traditional | Telesair, Inc. | 05/08/2025SE |
| K243394 | AF531 Oro-Nasal SE Face MaskCBK · Traditional | Respironics, Inc. | 12/30/2024SE |
| K233486 | 731 Series VentilatorCBK · Traditional | ZOLL Medical Corporation | 12/13/2024SE |
| K223120 | Ventoux VC2; Ventoux VC3CBK · Traditional | Flight Medical Innovations , Ltd. | 12/02/2024SE |
More from Flight Medical Innovations , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K253647 | Evita (V800); Evita (V600)CBK · Traditional | 05/07/2026SE |
| K242769 | VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)BTL · Traditional | 04/04/2025SE |
| K222822 | VentStar Helix dual heated (N) Plus (MP02650), VentStar Helix heated (N) Plus (MP02608)BZE · Traditional | 06/14/2023SE |
| K222207 | Babylog VN800, Babylog VN600CBK · Traditional | 05/16/2023SE |
| K221118 | CO2 Mainstream SensorCCK · Traditional | 04/05/2023SE |
| K162821 | Babyleo TN500FMZ · Traditional | 06/23/2017SE |
| K093633 | Infinity Acute Care System Workstation Critical CareCBK · Traditional | 03/30/2010SE |
Questions and answers
When was Evita V800, Evita V600 cleared by the FDA?
Evita V800, Evita V600 (K222024) received a 510(k) decision of Substantially Equivalent on May 16, 2023, 309 days after the submission was received.
What is the product code of K222024?
The FDA product code is CBK – Ventilator, Continuous, Facility Use, a Class II (moderate risk) device regulated under 21 CFR 868.5895.