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RESTING EKG ELECTRODE SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910494
510(k) Type
Traditional
Applicant
MEDTRONIC ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1991
Days to Decision
76 days

RESTING EKG ELECTRODE SERIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910494
510(k) Type
Traditional
Applicant
MEDTRONIC ANDOVER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/22/1991
Days to Decision
76 days