Theraflow Single Lumen and Theraflow Dual Lumen
FDA 510(k) K131023 · Medical Products, LLC
510(k) numberK131023
Submission
- Device name
- Theraflow Single Lumen and Theraflow Dual Lumen
- Applicant
- Medical Products, LLC
Indianapolis, IN, US - Received
- April 12, 2013
- Decision date
- October 11, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- NFB – Conserver, Oxygen
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5905
- Specialty
- Anesthesiology
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| K250322 | Respond OC Conserving Regulator (130-0800)NFB · Traditional | Responsive Respiratory | 07/24/2025SE |
| K220591 | ProximaNFB · Traditional | Dynasthetics, LLC | 12/15/2022SE |
| K221014 | Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileNFB · Traditional | Effortless Oxygen, LLC | 10/17/2022SE |
| K200401 | ApogeeNFB · Traditional | Incoba Ltd D/B/A Dynaris | 11/14/2020SE |
| K151506 | Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaNFB · Traditional | Salter Labs | 03/11/2016SE |
| K113111 | Chad Therapeutic Evolution Electronic Oxygen Conserver with MotionNFB · Special | Inovo, Inc. | 12/08/2011SE |
| K103392 | Chad Therapeutic Evolution Electronic Oxygen ConserverNFB · Special | Inovo, Inc. | 12/17/2010SE |
| K090421 | Model 350G Gas ConserverNFB · Traditional | Inspired Technologies, Inc. | 05/29/2009SE |
| K070740 | Chad Therapeutics Bonsai Model 800NFB · Special | Chad Therapeutics, Inc. | 05/07/2007SE |
| K060751 | Inovo, Inc. Accupulse Single Lumen Conserving RegulatorNFB · Traditional | Inovo, Inc. | 07/18/2006SE |
More from Inovo, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K981509 | Tempo IIILGZ · Traditional | 07/10/1998SE |
Questions and answers
When was Theraflow Single Lumen and Theraflow Dual Lumen cleared by the FDA?
Theraflow Single Lumen and Theraflow Dual Lumen (K131023) received a 510(k) decision of Substantially Equivalent on October 11, 2013, 182 days after the submission was received.
What is the product code of K131023?
The FDA product code is NFB – Conserver, Oxygen, a Class II (moderate risk) device regulated under 21 CFR 868.5905.