K-number	K761234
Device name	BEHRING LASER NEPHELOMETER
Applicant	Behring Diagnostics, Inc.
Product code	JZW
Device class	Class I
Decision date	Jun 7, 1990
Decision	Substantially Equivalent
Regulation	866.4540

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View the full FDA submission: accessdata.fda.gov

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BEHRING LASER NEPHELOMETER

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