4 results  1 of 1 

1 An evaluation of the Manufacturer And User Facility Device Experience database that inspired the United States Food and Drug Administration's Reclassification of transvaginal mesh
Jason M. Sandberg, Ian Gray, Amy Pearlman, Ryan P. Terlecki
Investig Clin Urol.2018;59(2):126-132.   Published online 2018 January 29     DOI: http://dx.doi.org/10.4111/icu.2018.59.2.126
      
2 A comparative clinical study on the accuracy and efficacy of Accumate® 1100, an infusion pump for patient-controlled analgesia
Kye-Min Kim, Gyu-Jeong Noh
Anesth Pain Med.2016;11(1):36-41.   Published online 2016 January 31     DOI: http://dx.doi.org/10.17085/apm.2016.11.1.36
      
3 Arrangements of the intravenous parallel infusions with anti-reflux valves decreasing occlusion alarm delay
Han Bum Joe, Bong-Ki Moon, Yeon-Ju Lee, Sang-Kee Min
Korean J Anesthesiol.2014;66(4):300-305.   Published online 2014 April 28     DOI: http://dx.doi.org/10.4097/kjae.2014.66.4.300
      
4 Electro-Mechanical Safety Testing of Portable ECG Devices for Home Healthcare Usage
Ju Hyun Kim, Eun Jeong Cho, Chung Ki Lee, Su Kang Park, Byung Chae Lee, Sun Kook Yoo
Healthc Inform Res.2010;16(1):30-35.   Published online 2010 March 31     DOI: http://dx.doi.org/10.4258/hir.2010.16.1.30
      

 1 of 1