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HYBRID ARCTICGEL PAD

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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