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PATHWAY II ELECTROMYOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K897132
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1991
Days to Decision
477 days

PATHWAY II ELECTROMYOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K897132
510(k) Type
Traditional
Applicant
THE PROMETHEUS GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/1991
Days to Decision
477 days