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MUSCLESENSE ELECTROMYOGRAPHY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K951350
510(k) Type
Traditional
Applicant
SMITH AND NEPHEW DONJOY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1995
Days to Decision
91 days
Submission Type
Summary

MUSCLESENSE ELECTROMYOGRAPHY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K951350
510(k) Type
Traditional
Applicant
SMITH AND NEPHEW DONJOY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/23/1995
Days to Decision
91 days
Submission Type
Summary