K-number	K802103
Device name	ECG RECALL & EDIT PRODUCT VERSION-A3601
Applicant	General Electric Co.
Product code	DSI
Device class	Class II
Decision date	Sep 26, 1980
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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ECG RECALL & EDIT PRODUCT VERSION-A3601

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