Exerciser, Resp., Deep Breathing
FDA 510(k) K780037 · Medical Technologies of Georgia
510(k) numberK780037
Submission
- Device name
- Exerciser, Resp., Deep Breathing
- Applicant
- Medical Technologies of Georgia
Mchenry, IL, US - Received
- January 9, 1978
- Decision date
- February 24, 1978
- 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 |
|---|---|---|
| K080878 | MTG Instant Cather (with and Without Kit), MTG Instant Cath Deluxe (with and Without Kit)KOD · Traditional | 07/17/2008SE |
| K973120 | Readycath CatheterGBM · Traditional | 02/25/1998SE |
| K952392 | Mli SetFPA · Traditional | 08/07/1995SE |
| K911129 | MMG Bile BagEXF · Traditional | 08/07/1991SE |
| K873136 | MMG Cath-N-PlaceKNX · Traditional | 09/09/1987SE |
| K871949 | MMG Delee Suction Catheter W/Mucous TrapBSY · Traditional | 06/15/1987SE |
| K854821 | MMG External Female CathetersKNX · Traditional | 04/24/1986SE |
| K854660 | The MMG Enteral Feeding Administration SetKNT · Traditional | 01/21/1986SE |
| K840839 | MMG Foley CatheterKOD · Traditional | 04/17/1984SE |
| K840897 | Oxygen TubingCAT · Traditional | 03/16/1984SE |
Questions and answers
When was Exerciser, Resp., Deep Breathing cleared by the FDA?
Exerciser, Resp., Deep Breathing (K780037) received a 510(k) decision of Substantially Equivalent on February 24, 1978, 46 days after the submission was received.
What is the product code of K780037?
The FDA product code is BWF – Spirometer, Therapeutic (Incentive), a Class II (moderate risk) device regulated under 21 CFR 868.5690.