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PATHWAY ELECTROMYOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K973537
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1997
Days to Decision
90 days
Submission Type
Statement

PATHWAY ELECTROMYOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K973537
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/1997
Days to Decision
90 days
Submission Type
Statement