Last synced on 14 November 2025 at 11:06 pm

K-STIK DEFIBRILLATION PADS

Page Type
Cleared 510(K)
510(k) Number
K863899
510(k) Type
Traditional
Applicant
KATECHO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1986
Days to Decision
36 days

K-STIK DEFIBRILLATION PADS

Page Type
Cleared 510(K)
510(k) Number
K863899
510(k) Type
Traditional
Applicant
KATECHO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1986
Days to Decision
36 days