K-number	K771447
Device name	PREGELLED DISP. EKG MONITORING ELECT-
Applicant	Hayes Products, Inc.
Product code	DRX
Device class	Class II
Decision date	Aug 4, 1977
Decision	Substantially Equivalent
Regulation	870.2360

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View the full FDA submission: accessdata.fda.gov

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PREGELLED DISP. EKG MONITORING ELECT-

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