6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
PENTAX BROCHOFIBERSCOPE MODEL FB-17D,
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
SMARTPILL GI MONITORING SYSTEM, VERSION 2.0
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Electrosurgical System (Electrosurgical Generator with Bipolar polypectomy snare combination and Single use electrosurgical knife combination accessories)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2014
NEXGEN MIS STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·October 12, 2012
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2010