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ZOLL E SERIES DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072923
510(k) Type
Traditional
Applicant
ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2008
Days to Decision
192 days
Submission Type
Summary

ZOLL E SERIES DEFIBRILLATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K072923
510(k) Type
Traditional
Applicant
ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2008
Days to Decision
192 days
Submission Type
Summary