K-number	K060815
Device name	JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT
Applicant	Bioform Medical, Inc.
Product code	MIX
Device class	Class II
Decision date	Apr 18, 2006
Decision	Substantially Equivalent
Regulation	874.3620

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View the full FDA submission: accessdata.fda.gov

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JULIESSE INJECTABLE LARYNGEAL AUGMENTATION IMPLANT

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