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SHOCK-PATCH ADULT DEFIBRILLATION PADS

Page Type
Cleared 510(K)
510(k) Number
K920086
510(k) Type
Traditional
Applicant
CARDIOTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1992
Days to Decision
26 days
Submission Type
Statement

SHOCK-PATCH ADULT DEFIBRILLATION PADS

Page Type
Cleared 510(K)
510(k) Number
K920086
510(k) Type
Traditional
Applicant
CARDIOTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1992
Days to Decision
26 days
Submission Type
Statement