K-number	K792383
Device name	KELMAN DIPSTICK
Applicant	V. Mueller O.V. Baxter Healthcare Corp.
Product code	HOE
Device class	Class I
Decision date	Dec 11, 1979
Decision	Substantially Equivalent
Regulation	886.4350

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Source

View the full FDA submission: accessdata.fda.gov

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KELMAN DIPSTICK

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