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GUIDEMIA

Page Type
Cleared 510(K)
510(k) Number
K121466
510(k) Type
Traditional
Applicant
Guidemia Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2012
Days to Decision
14 days
Submission Type
Statement

GUIDEMIA

Page Type
Cleared 510(K)
510(k) Number
K121466
510(k) Type
Traditional
Applicant
Guidemia Technologies, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2012
Days to Decision
14 days
Submission Type
Statement