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POWERTREK INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K972057
510(k) Type
Traditional
Applicant
Medtrek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
156 days
Submission Type
Statement

POWERTREK INSTRUMENTS

Page Type
Cleared 510(K)
510(k) Number
K972057
510(k) Type
Traditional
Applicant
Medtrek Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1997
Days to Decision
156 days
Submission Type
Statement