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MYOCARE PLUS DUAL CHANNEL STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K851046
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/1/1985
Days to Decision
109 days

MYOCARE PLUS DUAL CHANNEL STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K851046
510(k) Type
Traditional
Applicant
3M COMPANY
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/1/1985
Days to Decision
109 days