Ohio Volume Incentive Spirometer
FDA 510(k) K813476 · Airco/Ohio Medical Products
510(k) numberK813476
Submission
- Device name
- Ohio Volume Incentive Spirometer
- Applicant
- Airco/Ohio Medical Products
Mchenry, IL, US - Received
- December 1, 1981
- Decision date
- December 31, 1981
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BWF – Spirometer, Therapeutic (Incentive)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5690
- Specialty
- Anesthesiology
Other 510(k)s with product code BWF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K241152 | InSeeBWF · Traditional | Tidal Medical Technologies, LLC | 08/21/2025SE |
| K233855 | AllPEPBWF · Traditional | Enchant Tek Co. , Ltd. | 02/02/2024SE |
| K221058 | LungTrainer (MD2 & MD3)BWF · Traditional | Lung Trainers, LLC | 07/05/2023SE |
| K222018 | Breathe+BWF · Traditional | Peep Medical, LLC Dba Go2 Devices | 06/02/2023SE |
| K220565 | Hudson RCI Triflo II Incentive Deep Breathing ExerciserBWF · Traditional | Medline Industries, Inc. | 10/25/2022SE |
| K203378 | PulsehalerBWF · Traditional | Respinova, Ltd. | 03/31/2021SE |
| K192000 | D R Burton OxyPAPBWF · Traditional | D R Burton Healthcare, LLC | 02/19/2020SE |
| K181660 | Acapella Choice Blue Vibratory PEP DeviceBWF · Traditional | Smiths Medical | 10/24/2019SE |
| K183108 | Combined Aerobika OPEP and VersaPAP deviceBWF · Traditional | Trudell Medical International | 08/16/2019SE |
| K182847 | Hudson RCI Voldyne Volumetric ExerciserBWF · Traditional | Teleflexmedical, Inc. | 07/01/2019SE |
More from Teleflexmedical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K833459 | Coaxial Vol. Ventilator CircuitBZO · Traditional | 01/10/1984SE |
| K833452 | Ohio GMS AbsorberBSF · Traditional | 11/29/1983SE |
| K832418 | Ohio Temperature SimulatorFMZ · Traditional | 09/12/1983SE |
| K832565 | Ohio 5400 Volume MonitorBZK · Traditional | 09/01/1983SE |
| K832185 | Ohio Model 922 SpirometerBZG · Traditional | 08/12/1983SE |
| K830446 | Oxygen Monitor Ohio 5100CCL · Traditional | 03/24/1983SE |
| K822456 | Ohio V5A Anesthesia VentilatorCBK · Traditional | 09/21/1982SE |
| K812880 | Ohio Non-Reusable Tracheal Tube MajillBTR · Traditional | 11/24/1981SE |
| K812879 | Ohio Non-Reusable Tracheal Tube MurphyBTR · Traditional | 11/24/1981SE |
| K811413 | Dabc Nonconductive Pediat. Anesth. CirCAI · Traditional | 06/02/1981SE |
Questions and answers
When was Ohio Volume Incentive Spirometer cleared by the FDA?
Ohio Volume Incentive Spirometer (K813476) received a 510(k) decision of Substantially Equivalent on December 31, 1981, 30 days after the submission was received.
What is the product code of K813476?
The FDA product code is BWF – Spirometer, Therapeutic (Incentive), a Class II (moderate risk) device regulated under 21 CFR 868.5690.