K-number	K001146
Device name	GENYX FLEXIBLE INJECTION NEEEDLE
Applicant	Geny Medical, Inc.
Product code	FBK
Device class	Class II
Decision date	Jun 30, 2000
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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GENYX FLEXIBLE INJECTION NEEEDLE

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