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MODIFIED HEARTSTART DEFIBRILLATION ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K902429
510(k) Type
Traditional
Applicant
LAERDAL MFG. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
128 days

MODIFIED HEARTSTART DEFIBRILLATION ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K902429
510(k) Type
Traditional
Applicant
LAERDAL MFG. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1990
Days to Decision
128 days