K-number	K913941
Device name	PSG(TM) 20 GUAGE DOPPLER NEEDLE
Applicant	Peripheral Systems Group
Product code	ITX
Device class	Class II
Decision date	Feb 27, 1992
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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PSG(TM) 20 GUAGE DOPPLER NEEDLE

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