K-number	K860249
Device name	THE HOLTER REPORTER (TM)
Applicant	Applied Cardiac Systems
Product code	DPS
Device class	Class II
Decision date	Mar 11, 1986
Decision	Substantially Equivalent
Regulation	870.2340

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Source

View the full FDA submission: accessdata.fda.gov

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THE HOLTER REPORTER (TM)

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