K-number	K833782
Device name	SURGITEK ALL SILICONE INFECTION DOUBJ
Applicant	Surgitek
Product code	FAD
Device class	Class II
Decision date	Apr 2, 1984
Decision	Substantially Equivalent
Regulation	876.4620

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View the full FDA submission: accessdata.fda.gov

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SURGITEK ALL SILICONE INFECTION DOUBJ

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