K-number	K900519
Device name	CLASSIC ECG/STIMULATING NO. 1700 SERIES
Applicant	Classic Medical Products, Inc.
Product code	DRX
Device class	Class II
Decision date	Mar 19, 1990
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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CLASSIC ECG/STIMULATING NO. 1700 SERIES

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