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K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60

Page Type
Cleared 510(K)
510(k) Number
K981737
510(k) Type
Traditional
Applicant
Katecho, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1998
Days to Decision
205 days
Submission Type
Statement

K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60

Page Type
Cleared 510(K)
510(k) Number
K981737
510(k) Type
Traditional
Applicant
Katecho, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/1998
Days to Decision
205 days
Submission Type
Statement