APPALEAD GW+03XXXXXXR SERIES (K003394) — FDA 510(k) Clearance | Predicase

K-number	K003394
Device name	APPALEAD GW+03XXXXXXR SERIES
Applicant	Nipro Medical Corp.
Product code	DQX
Device class	Class II
Decision date	Jan 30, 2001
Decision	Substantially Equivalent
Regulation	870.1330

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Source

View the full FDA submission: accessdata.fda.gov

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