K-number	K930508
Device name	HIFLO FILTERED INSUFFLATION TUBING
Applicant	W. J. Medical Instruments, Inc.
Product code	FCX
Device class	Class II
Decision date	Jun 25, 1993
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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HIFLO FILTERED INSUFFLATION TUBING

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