K-number	K894161
Device name	ASC-950 ECG AMPLIFIER
Applicant	Astro-Med, Inc.
Product code	DRR
Device class	Class II
Decision date	Aug 3, 1989
Decision	Substantially Equivalent
Regulation	870.2050

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View the full FDA submission: accessdata.fda.gov

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ASC-950 ECG AMPLIFIER

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