Medi-Stim Veriq System, Model VQ1001 - VQ4122
FDA 510(k) K040228 · Medi-Stim A/S
510(k) numberK040228
Submission
- Device name
- Medi-Stim Veriq System, Model VQ1001 - VQ4122
- Applicant
- Medi-Stim A/S
Brooklyn Park, MN, US - Received
- February 2, 2004
- Decision date
- April 29, 2004
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DPW – Flowmeter, Blood, Cardiovascular
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2100
- Specialty
- Cardiovascular
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| K243852 | Elfor-LDPW · Traditional | Elfi-Tech , Ltd. | 04/14/2025SE |
| K241583 | VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Charger…DPW · Special | Remington Medical, Inc. | 08/30/2024SE |
| K223843 | FloPatch FP120DPW · Traditional | Flosonics Medical | 05/03/2023SE |
| K222242 | FloPatch FP120DPW · Traditional | Flosonics Medical | 12/09/2022SE |
| K213974 | GEM FLOW COUPLER Monitor (GEM1020M-2)DPW · Special | Synovis Micro Companies Alliance, Inc. | 04/20/2022SE |
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More from Remington Medical, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K992305 | Medi-Stim Butterfly Flowmeter, Model BF1000-BF2004ITX · Traditional | 09/08/1999SE |
Questions and answers
When was Medi-Stim Veriq System, Model VQ1001 - VQ4122 cleared by the FDA?
Medi-Stim Veriq System, Model VQ1001 - VQ4122 (K040228) received a 510(k) decision of Substantially Equivalent on April 29, 2004, 87 days after the submission was received.
What is the product code of K040228?
The FDA product code is DPW – Flowmeter, Blood, Cardiovascular, a Class II (moderate risk) device regulated under 21 CFR 870.2100.