FDA 510(k) Applications Submitted by Kit Cariquitan

FDA 510(k) Number Submission Date Device Name Applicant
K090070 01/12/2009 INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM INVUITY, INC.
K110228 01/26/2011 NIDEK MULTICOLOR LASER PHOTOCOAGULATOR NIDEK INCORPORATED
K100445 02/17/2010 KLASSIC HD HIP SYSTEM TOTAL JOINT ORTHOPEDICS, INC.
K110541 02/25/2011 FIGURE 8 STERNOTOMY CLOSURE DEVICE FIGURE 8 SURGICAL, INCORPORATED
K111187 04/27/2011 PATCH, PLEDGET AND INTRACARDIAC CORMATRIX CARDIOVASCULAR, INC.
K111338 05/12/2011 WILDCAT CATHETER AVINGER, INC.
K212392 08/02/2021 Intri24 Sheath Inari Medical, Inc.
K142241 08/13/2014 LARIAT sulture Delivery Device SENTREHEART INC.
K072297 08/17/2007 BOOMERANG CATALYST/BOOMERANG CATALYST II SYSTEM CARDIVA MEDICAL, INC.
K102329 08/17/2010 NANOKNIFE SYSTEM ANGIODYNAMICS, INC.
K082930 10/01/2008 CARDIVA CATALYST III SYSTEM WITH PROTAMINE SULFATE CARDIVA MEDICAL, INC.
K213402 10/18/2021 Triever24, Triever20 Inari Medical
K153096 10/26/2015 LARIAT RS Suture Delivery Device SentreHEART, Inc.
K063349 11/06/2006 CORMATRIX PATCH FOR CARDIAC TISSUE REPAIR CORMATRIX CARDIOVASCULAR, INC.
K103428 11/22/2010 THE ARTAS SYSTEM FROM RESTORATION ROBOTICS RESTORATION ROBOTICS, INC


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