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HEARTSTRAMELECTRODE ADAPTER(EA-XX SERIES)/HEARTSTRAM DEFIBRILLATION PADS WITH PREATTACHED ELECTRODE ADAPTER(DP-EAXX)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972418
510(k) Type
Traditional
Applicant
Heartstream, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1997
Days to Decision
90 days
Submission Type
Summary

HEARTSTRAMELECTRODE ADAPTER(EA-XX SERIES)/HEARTSTRAM DEFIBRILLATION PADS WITH PREATTACHED ELECTRODE ADAPTER(DP-EAXX)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K972418
510(k) Type
Traditional
Applicant
Heartstream, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1997
Days to Decision
90 days
Submission Type
Summary