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ULTRAHESIVE II POSTOP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K862028
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1986
Days to Decision
65 days

ULTRAHESIVE II POSTOP ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K862028
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1986
Days to Decision
65 days