K-number	K915808
Device name	AQUEOUS PARACENTESIS PIPET
Applicant	Visitec Co.
Product code	KYG
Device class	Class I
Decision date	Mar 19, 1992
Decision	Substantially Equivalent
Regulation	886.4360

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Source

View the full FDA submission: accessdata.fda.gov

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AQUEOUS PARACENTESIS PIPET

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