K-number	K950574
Device name	NEEDLE/CANNULA
Applicant	Tri-Med Specialties, Inc.
Product code	LRO
Device class	Class II
Decision date	Feb 24, 1995
Decision	Substantially Equivalent — Kit Device
Regulation	878.4370

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View the full FDA submission: accessdata.fda.gov

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NEEDLE/CANNULA

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