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ECG RECALL & EDIT PRODUCT VERSION-A3601

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802103
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
23 days

ECG RECALL & EDIT PRODUCT VERSION-A3601

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802103
510(k) Type
Traditional
Applicant
GENERAL ELECTRIC CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/1980
Days to Decision
23 days