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FDA 510(k) Applications Submitted by SCOTT KARLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070129
01/16/2007
SONOTIP II ULTRASOUND NEEDLE SYSTEM
MEDI-GLOBE CORPORATION
K010549
02/26/2001
BILIARY AND PANCREATIC ENDOPROSTHESES (STENTS)
MEDI-GLOBE CORP.
K011261
04/25/2001
STONE EXTRACTOR BALLOON CATHETER
MEDI-GLOBE CORP.
K091257
04/29/2009
MEDI-GLOBE SONOTIP II EBUS-TBNA NEEDLE SYSTEM
MEDI-GLOBE CORPORATION
K061222
05/02/2006
INJECTRA INJECTION NEEDLE
MEDI-GLOBE CORP.
K051247
05/16/2005
SONOTIP II ULTRASOUND NEEDLE SYSTEM
MEDI-GLOBE CORP.
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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