FDA 510(k) Applications Submitted by Medi-Globe Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K070129 01/16/2007 SONOTIP II ULTRASOUND NEEDLE SYSTEM MEDI-GLOBE CORPORATION
K091257 04/29/2009 MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM MEDI-GLOBE CORPORATION
K061684 06/15/2006 MEDI-GLOBE ROTA-CUT SPHINCTEROTOME MEDI-GLOBE CORPORATION
K142258 08/14/2014 PolyCatch Retrieval Device Medi-Globe Corporation
K153264 11/12/2015 EasyPass Guidewire MEDI-GLOBE CORPORATION
K133763 12/11/2013 SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM MEDI-GLOBE CORPORATION
K083802 12/22/2008 SONOTIP II 25-GAUGE ULTRASOUND NEEDLE SYSTEM, MODELS GUS-01-18-025 AND GUS-01-27-025 MEDI-GLOBE CORPORATION


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