K-number	K780484
Device name	SILASTIC BRAND PENILE IMPLANT
Applicant	Dow Corning Corp. Healthcare Industries Materials
Product code	FIQ
Device class	Class II
Decision date	Jul 17, 1978
Decision	Substantially Equivalent
Regulation	876.5540

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View the full FDA submission: accessdata.fda.gov

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SILASTIC BRAND PENILE IMPLANT

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