Home › Device types › MQS
System, Hemodialysis, Access Recirculation Monitoring
FDA product code MQS · Class 2 · Gastroenterology, Urology
13
Registered devices
271
Adverse events
1
Recalls
18
510(k) clearances
Devices with this code
Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Smart Anemia Manager (SAM) — Dosis Inc.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.Transonic — TRANSONIC SYSTEMS INC.PhySoft AMS — PHYSICIAN SOFTWARE SYSTEMS, LLCTransonic — TRANSONIC SYSTEMS INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-02-17 | Transonic Systems Inc | Customer unable to obtain measurements due to the device seeing no flow or irrelevant flow condition during dialysis procedures. The user saw a zero or a very |
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