FDA 510(k) Applications Submitted by CHRIS RADL

FDA 510(k) Number Submission Date Device Name Applicant
K150781 03/25/2015 Tissue Removal Pouch BOEHRINGER LABORATORIES, LLC
K151990 07/20/2015 Tissue Removal System BOEHRINGER LABORATORIES LLC
K060277 02/02/2006 BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM BOEHRINGER LABORATORIES
K020538 02/19/2002 BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES BOEHRINGER LABORATORIES
K061788 06/26/2006 BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM BOEHRINGER LABORATORIES
K130483 02/25/2013 BOEHRINGER GASTRIC SIZING TUBE BOEHRINGER LABORATORIES, LLC


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