K-number	K011488
Device name	SPIRABRUSH CX BIOPSY INSTRUMENT
Applicant	Trylon Corp.
Product code	HFB
Device class	Class I
Decision date	Feb 22, 2002
Decision	Substantially Equivalent
Regulation	884.4530

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View the full FDA submission: accessdata.fda.gov

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SPIRABRUSH CX BIOPSY INSTRUMENT

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