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ELECTRODE, ELECTROFLEX

Page Type
Cleared 510(K)
510(k) Number
K790316
510(k) Type
Traditional
Applicant
ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1979
Days to Decision
40 days

ELECTRODE, ELECTROFLEX

Page Type
Cleared 510(K)
510(k) Number
K790316
510(k) Type
Traditional
Applicant
ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1979
Days to Decision
40 days