K-number	K913726
Device name	DURALIFE(TM)
Applicant	Dhd Diemolding Healthcare Div.
Product code	BZA
Device class	Class I
Decision date	Feb 7, 1992
Decision	Substantially Equivalent
Regulation	868.5810

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View the full FDA submission: accessdata.fda.gov

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DURALIFE(TM)

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