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HYBRID ARCTICGEL PAD

Page Type
Cleared 510(K)
510(k) Number
K120849
510(k) Type
Traditional
Applicant
Medivance, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2012
Days to Decision
122 days
Submission Type
Summary

HYBRID ARCTICGEL PAD

Page Type
Cleared 510(K)
510(k) Number
K120849
510(k) Type
Traditional
Applicant
Medivance, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2012
Days to Decision
122 days
Submission Type
Summary