K-number	K040919
Device name	NUCLEOTOME PROBE SET, MODEL 21200
Applicant	Clarus Medical, LLC
Product code	HRX
Device class	Class II
Decision date	Jun 1, 2004
Decision	Substantially Equivalent
Regulation	888.1100

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View the full FDA submission: accessdata.fda.gov

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NUCLEOTOME PROBE SET, MODEL 21200

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