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SKINSENSE POLYISOPRENE UNDERGLOVE

Page Type
Cleared 510(K)
510(k) Number
K081180
510(k) Type
Traditional
Applicant
MOLNLYCKE HEALTH CARE US, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2008
Days to Decision
123 days
Submission Type
Summary

SKINSENSE POLYISOPRENE UNDERGLOVE

Page Type
Cleared 510(K)
510(k) Number
K081180
510(k) Type
Traditional
Applicant
MOLNLYCKE HEALTH CARE US, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/26/2008
Days to Decision
123 days
Submission Type
Summary