K-number	K960094
Device name	REFLECTION DUAL DIMENSION SHELL
Applicant	Smith & Nephew Richards, Inc.
Product code	MBL
Device class	Class II
Decision date	Mar 27, 1996
Decision	Substantially Equivalent
Regulation	888.3358

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View the full FDA submission: accessdata.fda.gov

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REFLECTION DUAL DIMENSION SHELL

Everything you need for a 510(k) submission. Nothing you don't.