K-number	K900051
Device name	MOORE TYPE ENDO PROSTHESIS
Applicant	Lima Intl. Corp.
Product code	KWY
Device class	Class II
Decision date	Oct 3, 1990
Decision	Substantially Equivalent
Regulation	888.3390

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View the full FDA submission: accessdata.fda.gov

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MOORE TYPE ENDO PROSTHESIS

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