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DC200 DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K910634
510(k) Type
Traditional
Applicant
SIEMENS BURDICK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
161 days

DC200 DEFIBRILLATOR

Page Type
Cleared 510(K)
510(k) Number
K910634
510(k) Type
Traditional
Applicant
SIEMENS BURDICK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
161 days