K-number	K971480
Device name	DURALASTIC I AND DURALASTIC II
Applicant	Allied Biomedical Corp.
Product code	MIB
Device class	Class II
Decision date	May 28, 1997
Decision	Substantially Equivalent
Regulation	874.3620

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View the full FDA submission: accessdata.fda.gov

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DURALASTIC I AND DURALASTIC II

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