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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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