K-number	K855089
Device name	PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505
Applicant	Dlp, Inc.
Product code	DQX
Device class	Class II
Decision date	Feb 18, 1986
Decision	Substantially Equivalent
Regulation	870.1330

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PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505

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