K-number	K212379
Device name	N Latex FLC kappa, N Latex FLC lambda
Applicant	Siemens Healthcare Diagnostics Products GmbH
Product code	DFH
Device class	Class II
Decision date	Mar 2, 2022
Decision	Substantially Equivalent
Regulation	866.5550

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Source

View the full FDA submission: accessdata.fda.gov

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N Latex FLC kappa, N Latex FLC lambda

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