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TRANSCURE, MODEL 2910

Page Type
Cleared 510(K)
510(k) Number
K022862
510(k) Type
Traditional
Applicant
KINETIC INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
51 days
Submission Type
Statement

TRANSCURE, MODEL 2910

Page Type
Cleared 510(K)
510(k) Number
K022862
510(k) Type
Traditional
Applicant
KINETIC INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2002
Days to Decision
51 days
Submission Type
Statement