K-number	K831829
Device name	KARICKHOFF FLYING CORPUSCLE VIEWER
Applicant	Surgidev Corp.
Product code	HIX
Device class	Class I
Decision date	Oct 19, 1983
Decision	Substantially Equivalent
Regulation	886.1435

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View the full FDA submission: accessdata.fda.gov

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KARICKHOFF FLYING CORPUSCLE VIEWER

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