K-number	K930357
Device name	ACCESSORY TO UNIVERSAL OCTOPAQUE
Applicant	Octostop, Inc.
Product code	KXH
Device class	Class I
Decision date	Jul 13, 1993
Decision	Substantially Equivalent
Regulation	892.1830

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View the full FDA submission: accessdata.fda.gov

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ACCESSORY TO UNIVERSAL OCTOPAQUE

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