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FASTRACE III, ECG ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K860636
510(k) Type
Traditional
Applicant
ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1986
Days to Decision
77 days

FASTRACE III, ECG ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K860636
510(k) Type
Traditional
Applicant
ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1986
Days to Decision
77 days