Eflow Electronic Inhaler/Nebulizer
FDA 510(k) K033833 · Pari Innovative Manufacturers, Inc.
510(k) numberK033833
Submission
- Device name
- Eflow Electronic Inhaler/Nebulizer
- Applicant
- Pari Innovative Manufacturers, Inc.
Midlothian, VA, US - Received
- December 10, 2003
- Decision date
- May 5, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
- Third-party review
- Yes
Device classification
- Product code
- CAF – Nebulizer (Direct Patient Interface)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.5630
- Specialty
- Anesthesiology
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| K260270 | FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)CAF · Traditional | FindAir Sp. z o.o. | 06/02/2026SE |
| K251572 | eRapid with eTrack SystemCAF · Traditional | Pari Respiratory Equipment, Inc. | 12/19/2025SE |
| K251659 | Mesh Nebulizer (H6)CAF · Traditional | Qingdao Future Medical Technology Co., Ltd. | 11/14/2025SE |
| K244035 | Portable mesh nebulizer (JM821)CAF · Traditional | Shenzhen Jermei Medical Device Technology Co.… | 09/19/2025SE |
| K243468 | Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer…CAF · Traditional | Joytech Healthcare Co. , Ltd. | 07/02/2025SE |
| K250022 | HeroTracker SenseCAF · Traditional | Voluntis | 06/30/2025SE |
| K250583 | AdheResp Smart Breath-actuated Mesh NebulizerCAF · Traditional | Hcmed Innovations Co., Ltd. | 06/20/2025SE |
| K242354 | AllNEBCAF · Traditional | Enchant Tek Co. , Ltd. | 04/29/2025SE |
| K233553 | MiniSpacer® 1024, 1025, 1543 and 1024A, 1025A, 1543A Dual Spray MDI AdapterCAF · Special | Thayer Medical Corporation | 06/18/2024SE |
| K232507 | Aerogen®Solo Nebulizer SystemCAF · Traditional | Aerogen, Ltd. | 05/10/2024SE |
More from Aerogen, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K072670 | Modification to: Eflow Electronic Inhaler/NebulizerCAF · Special | 12/13/2007SE |
| K072982 | Pari Hydrate VBTT · Traditional | 11/29/2007SE |
| K070498 | Hyper SalCAF · Traditional | 04/26/2007SE |
| K070107 | Pari Hydrate GBTT · Traditional | 02/23/2007SE |
| K062158 | LC Sprint StarCAF · Traditional | 08/28/2006SE |
| K061381 | LC Star with Nasal AdapterCAF · Traditional | 06/02/2006SE |
| K060357 | Trek S Nebulizer CompressorCAF · Traditional | 04/05/2006SE |
| K060399 | LC Sprint NebulizerCAF · Traditional | 03/02/2006SE |
| K020944 | Vortex Valved Holding ChamberCAF · Traditional | 05/09/2002SE |
Questions and answers
When was Eflow Electronic Inhaler/Nebulizer cleared by the FDA?
Eflow Electronic Inhaler/Nebulizer (K033833) received a 510(k) decision of Substantially Equivalent on May 5, 2004, 147 days after the submission was received.
What is the product code of K033833?
The FDA product code is CAF – Nebulizer (Direct Patient Interface), a Class II (moderate risk) device regulated under 21 CFR 868.5630.