K-number	K911292
Device name	SCHNEIDER WALLSTENT(R)
Applicant	Pfizer Hospital Products Group, Inc.
Product code	FGE
Device class	Class II
Decision date	May 1, 1991
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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SCHNEIDER WALLSTENT(R)

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