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FDA to radiologists: stop using any Multidata Systems devices

dotmed.com October 28, 2016

At least two devices distributed in U.S. without FDA approval. There have been at least two Multidata medical devices that the company manufactured and distributed in the United States for which FDA never received nor reviewed 510(k) premarket notifications.

FDA radiation technology therapy treatment ultrasound

Implementing a Bedside Percutaneous Tracheostomy and Ultrasound Gastrostomy Team Reduces Length of Stay and Hospital Costs

Protocolized Fluid Balance Neutralization During CRRT

How I Perform Diaphragmatic Ultrasound in the ICU

COVID-19 and the Cardiovascular System: From Pathophysiology to Clinical Management

COVID-19 and the Cardiovascular System: From Pathophysiology to Clinical Management

Clinical Application of Mechanical Ventilation

Hematologic Challenges in the Critically Ill

Spillover: Animal Infections and the Next Human Pandemic

Prediction and Management of Severe Acute Pancreatitis

Emergency Department Resuscitation of the Critically Ill

Perioperative Hemodynamic Monitoring and Goal Directed Therapy: From Theory to Practice

Workbook on Hemodynamic Management

Hemodynamic Monitoring Using Echocardiography in the Critically Ill

Bedside Procedures in the ICU

Trauma Team Dynamics: A Trauma Crisis Resource Management Manual

Evidence-Based Critical Care: A Case Study Approach

Clinical Examination Skills in the Adult Critically Ill Patient

Severe Trauma and Sepsis: Organ Damage and Tissue Repair

Moderate and Deep Sedation in Clinical Practice

Basics of Mechanical Ventilation