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ACMI BIPOLAR HEMOSTATIC ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K803214
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1981
Days to Decision
28 days

ACMI BIPOLAR HEMOSTATIC ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K803214
510(k) Type
Traditional
Applicant
AMERICAN CYSTOCOPE MAKERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1981
Days to Decision
28 days