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SOLID GEL PAD

Page Type
Cleared 510(K)
510(k) Number
K131905
510(k) Type
Traditional
Applicant
BLUEMTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2013
Days to Decision
22 days
Submission Type
Summary

SOLID GEL PAD

Page Type
Cleared 510(K)
510(k) Number
K131905
510(k) Type
Traditional
Applicant
BLUEMTECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2013
Days to Decision
22 days
Submission Type
Summary