K-number	K911118
Device name	DTF-1000LL,DTF-1000
Applicant	Cp Medical
Product code	EIB
Device class	Class I
Decision date	Nov 20, 1991
Decision	Substantially Equivalent
Regulation	872.4565

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View the full FDA submission: accessdata.fda.gov

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DTF-1000LL,DTF-1000

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