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SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR; EXTERNAL DEFIBRILLATION PADS (ELECTRODES) DDP-100; BATTERY PACK 1200MAH; BA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013896
510(k) Type
Traditional
Applicant
DEFIBTECH, LLC
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
6/19/2002
Days to Decision
208 days

SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR; EXTERNAL DEFIBRILLATION PADS (ELECTRODES) DDP-100; BATTERY PACK 1200MAH; BA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013896
510(k) Type
Traditional
Applicant
DEFIBTECH, LLC
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
6/19/2002
Days to Decision
208 days