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PATHWAY II ELECTROMYOGRAPH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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