Genesis BLS
FDA 510(k) K983643 · O-Two Systems Intl., Inc.
510(k) numberK983643
Submission
- Device name
- Genesis BLS
- Applicant
- O-Two Systems Intl., Inc.
Mississauga, CA - Received
- October 16, 1998
- Decision date
- October 29, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 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 |
| K141595 | O-Two E700,O-TWO E600,O-TWO E500BTL · Traditional | O-Two Medical Technologies, Inc. | 03/16/2015SE |
| K142096 | T-Piece ResuscitatorBTL · Traditional | Mercury Medical | 10/17/2014SE |
More from Mercury Medical
| 510(k) | Device | Decision |
|---|---|---|
| K991195 | Carevent BLS, Carevent Bls+, Carevent Als, Carevent Als+, and Carevent AtvBTL · Special | 04/22/1999SE |
| K983857 | Autovent 1500BTL · Special | 11/04/1998SE |
| K983785 | Autovent 1000BTL · Special | 10/29/1998SE |
| K983705 | Emt ResuscitatorBTL · Special | 10/29/1998SE |
| K960995 | CPR Bio-Barrier FacesheildCBP · Traditional | 01/07/1997SE |
| K940712 | PPM IIICBP · Traditional | 11/14/1994SE |
| K940927 | Rescue BreatherCBP · Traditional | 10/14/1994SE |
| K932170 | Flynnr Genesis II A/C, A/O and IdlhBTL · Traditional | 10/25/1993SE |
| K922810 | OdysseyBTM · Traditional | 01/22/1993SE |
| K913039 | Fllynn(R) Genesis AcBTL · Traditional | 08/25/1992SE |
Questions and answers
When was Genesis BLS cleared by the FDA?
Genesis BLS (K983643) received a 510(k) decision of Substantially Equivalent on October 29, 1998, 13 days after the submission was received.
What is the product code of K983643?
The FDA product code is BTL – Ventilator, Emergency, Powered (Resuscitator), a Class II (moderate risk) device regulated under 21 CFR 868.5925.