Medi-Globe Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153264EasyPass GuidewireMay 19, 2016
K142258PolyCatch Retrieval DeviceSeptember 30, 2014
K133763SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEMMay 15, 2014
K091257MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEMMay 8, 2009
K083802SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025March 20, 2009
K070129SONOTIP II ULTRASOUND NEEDLE SYSTEMJanuary 31, 2007
K061684MEDI-GLOBE ROTA-CUT SPHINCTEROTOMEJune 27, 2006