K-number	K851274
Device name	OHMEDA MODEL 0001/0003 RECORDER
Applicant	Ohmeda Medical
Product code	DSF
Device class	Class I
Decision date	May 15, 1985
Decision	Substantially Equivalent
Regulation	870.2810

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View the full FDA submission: accessdata.fda.gov

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OHMEDA MODEL 0001/0003 RECORDER

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