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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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