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ACIST RXi® Mini Navvus Interface
ACIST MEDICAL SYSTEMS, INC. · Model 018592 · UDI-DI 10841716101790
DRQ
Prescription
1
510(k) clearances
51
Adverse events
1
Recalls
36
Facilities
Description
RXi Mini Navvus Interface p/n 701600-002
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-06-02 | Boston Scientific Corporation | Boston Scientific has received complaints indicating that, when using the blood pressure (BP) channels on the CLEARSIGN II Amplifier, the surface Electrocardiogram (ECG) channels b |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.