Tiva
FDA 510(k) K142946 · Velano Vascular, Inc.
510(k) numberK142946
Submission
- Device name
- Tiva
- Applicant
- Velano Vascular, Inc.
Philadelphia, PA, US - Received
- October 10, 2014
- Decision date
- January 8, 2015
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1675
- Specialty
- Clinical Chemistry
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| K252899 | Female Culture Device; Male Culture Device; Transfer Device; Access DeviceJKA · Traditional | Zhejiang Kindly Medical Device Co., Ltd. | 06/02/2026SE |
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| K252506 | BD Vacutainer® Safety-Lok Blood Collection Set; BD Vacutainer® Safety-Lok Blood…JKA · Traditional | Becton, Dickinson and Company | 04/10/2026SE |
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| K251812 | Steripath® Flow Blood Collection SystemJKA · Traditional | Magnolia Medical Technologies | 09/25/2025SE |
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| K250961 | Blood collection tube holdersJKA · Traditional | Promisemed Hangzhou Meditech Co., Ltd. | 06/04/2025SE |
| K244047 | Navi Needle-free Blood Collection Device (VNC20500FG, VNC22500FG, VNC24500FG)JKA · Traditional | Venocare, Inc. | 05/23/2025SE |
| K250907 | Sol-Guard TM XtraThin Safety Pull-Button Blood Collection SetJKA · Special | Sol-Millennium Medical, Inc. | 04/30/2025SE |
More from Sol-Millennium Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K201237 | Velano Vascular Blood Collection AdapterJKA · Traditional | 10/03/2022SE |
| K200439 | Velano ExT Extension SetFPA · Traditional | 02/23/2021SE |
| K193569 | Pivo(Tm)JKA · Special | 01/21/2020SE |
| K190604 | PivoJKA · Special | 05/13/2019SE |
| K182897 | Velano Vascular Q2 Extension SetFPA · Traditional | 03/26/2019SE |
| K163508 | PivoJKA · Special | 02/09/2017SE |
| K152924 | Tiva¿JKA · Traditional | 01/07/2016SE |
Questions and answers
When was Tiva cleared by the FDA?
Tiva (K142946) received a 510(k) decision of Substantially Equivalent on January 8, 2015, 90 days after the submission was received.
What is the product code of K142946?
The FDA product code is JKA – Tubes, Vials, Systems, Serum Separators, Blood Collection, a Class II (moderate risk) device regulated under 21 CFR 862.1675.