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VESISCAN

Page Type
Cleared 510(K)
510(k) Number
K093485
510(k) Type
Traditional
Applicant
LIFE-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
127 days
Submission Type
Statement

VESISCAN

Page Type
Cleared 510(K)
510(k) Number
K093485
510(k) Type
Traditional
Applicant
LIFE-TECH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2010
Days to Decision
127 days
Submission Type
Statement