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MUSCLESENSE II CLINICAL ELECTROMYOGRAPHY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970051
510(k) Type
Traditional
Applicant
SMITH AND NEPHEW DONJOY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1997
Days to Decision
184 days
Submission Type
Summary

MUSCLESENSE II CLINICAL ELECTROMYOGRAPHY DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K970051
510(k) Type
Traditional
Applicant
SMITH AND NEPHEW DONJOY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1997
Days to Decision
184 days
Submission Type
Summary