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MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K900169
510(k) Type
Traditional
Applicant
LAERDAL MFG. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
14 days

MODIFIED HEARTSTART 2000 DEFIBRILLATION ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K900169
510(k) Type
Traditional
Applicant
LAERDAL MFG. CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1990
Days to Decision
14 days