K-number	K080040
Device name	ORTHO ALL-FLEX DIAPHRAGM
Applicant	Johnson & Johnson Produtos Profissionais Ltda.
Product code	HDW
Device class	Class II
Decision date	Aug 25, 2008
Decision	Substantially Equivalent
Regulation	884.5350

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Source

View the full FDA submission: accessdata.fda.gov

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ORTHO ALL-FLEX DIAPHRAGM

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