Oneflow FVC, Oneflow FVC (Kit), Oneflow FVC Screen
FDA 510(k) K042058 · Clement Clarke Intl., Ltd.
510(k) numberK042058
Submission
- Device name
- Oneflow FVC, Oneflow FVC (Kit), Oneflow FVC Screen
- Applicant
- Clement Clarke Intl., Ltd.
Harlow, GB - Received
- July 30, 2004
- Decision date
- March 23, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- BZG – Spirometer, Diagnostic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.1840
- Specialty
- Anesthesiology
Other 510(k)s with product code BZG
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251777 | MESI mTABLET SPIROBZG · Traditional | Mesi D.O.O. | 03/02/2026SE |
| K241843 | TD-7301 Spirometer (TD-7301)BZG · Traditional | Gostar Co., Ltd. | 11/20/2024SE |
| K231416 | Air Next (NVD-02)BZG · Traditional | Nuvoair AB | 01/18/2024SE |
| K230501 | Spirobank OxiBZG · Traditional | Mir Medical International Research USA | 12/15/2023SE |
| K230178 | EasyOne Sky SpirometerBZG · Traditional | Ndd Medizintechnik AG | 10/19/2023SE |
| K222525 | Alveoair Digital SpirometerBZG · Traditional | Roundworks Technologies Private Limited | 08/28/2023SE |
| K222443 | Air Smart Extra SpirometerBZG · Traditional | Feellife Health, Inc. | 08/09/2023SE |
| K213754 | SpiroHome Personal, SpiroHome ClinicBZG · Traditional | Inofab Saglik Teknolojileri A.S | 06/12/2023SE |
| K213872 | ComPAS2BZG · Traditional | Morgan Scientific, Inc. | 07/15/2022SE |
| K212938 | Vitalograph Model 6000 AlphaBZG · Traditional | Vitalograph Ireland, Ltd. | 01/26/2022SE |
More from Vitalograph Ireland, Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K053156 | Mini-Wright Digital, Model 3120001BZH · Traditional | 01/31/2006SE |
| K000368 | Eyecap Imaging SystemHKI · Traditional | 05/04/2000SE |
| K982334 | Airzone Peak FlowmeterBZH · Traditional | 01/14/1999SE |
| K980960 | In-Check Inspiratory FlowmeterBZH · Traditional | 06/10/1998SE |
| K962074 | VM Plus Peak FlowmeterBZH · Traditional | 01/02/1997SE |
Questions and answers
When was Oneflow FVC, Oneflow FVC (Kit), Oneflow FVC Screen cleared by the FDA?
Oneflow FVC, Oneflow FVC (Kit), Oneflow FVC Screen (K042058) received a 510(k) decision of Substantially Equivalent on March 23, 2005, 236 days after the submission was received.
What is the product code of K042058?
The FDA product code is BZG – Spirometer, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 868.1840.