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ZOLL PD2000 PACEMAKER/ADVISORY DEFIBRILLATOR, MODEL PD2000, ZOLL D2000 ADVISORY DEFIBRILLATOR, MODEL D2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950856
510(k) Type
Traditional
Applicant
ZOLL MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1995
Days to Decision
305 days
Submission Type
Statement

ZOLL PD2000 PACEMAKER/ADVISORY DEFIBRILLATOR, MODEL PD2000, ZOLL D2000 ADVISORY DEFIBRILLATOR, MODEL D2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950856
510(k) Type
Traditional
Applicant
ZOLL MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1995
Days to Decision
305 days
Submission Type
Statement