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MYOTEST NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K823583
510(k) Type
Traditional
Applicant
PROTHIA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
24 days

MYOTEST NERVE STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K823583
510(k) Type
Traditional
Applicant
PROTHIA USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
24 days