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PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960761
510(k) Type
Traditional
Applicant
The Prometheus Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1996
Days to Decision
163 days
Submission Type
Statement

PATHWAY ELECTROMYOGRAPH MODEL TR-10 & TR-20

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K960761
510(k) Type
Traditional
Applicant
The Prometheus Group
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/1996
Days to Decision
163 days
Submission Type
Statement