FDA 510(k) Applications Submitted by MOLNLYCKE HEALTHCARE, US LLC

FDA 510(k) Number Submission Date Device Name Applicant
K111413 05/20/2011 BIOGEL (R) INDICATOR (R) UNDERGLOVE MOLNLYCKE HEALTHCARE, US LLC
K112089 07/21/2011 BIOGEL ORTHOPOR BROWN SURGICAL GLOVE MOLNLYCKE HEALTHCARE, US LLC
K071465 05/29/2007 BIOGEL ORTHOPAEDIC SURGICAL GLOVE WITH NON-PRYOGENIC STATEMENT MOLNLYCKE HEALTHCARE, US LLC
K071700 06/21/2007 BIOGEL SENSOR SURGEON'S GLOVE WITH NON-PYROGENIC STATEMENT MOLNLYCKE HEALTHCARE, US LLC


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