K-number	K851971
Device name	SERIES 7000/HOLTER RECORDER
Applicant	Pfizer, Inc.
Product code	DSH
Device class	Class II
Decision date	Jun 20, 1985
Decision	Substantially Equivalent
Regulation	870.2800

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View the full FDA submission: accessdata.fda.gov

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SERIES 7000/HOLTER RECORDER

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