EMG TRITON -COMP,MODEL NCA01-XXX SERIES (K072634) — FDA 510(k) Clearance | Predicase

K-number	K072634
Device name	EMG TRITON -COMP,MODEL NCA01-XXX SERIES
Applicant	Emg Technology Co., Ltd.
Product code	BTI
Device class	Class II
Decision date	Nov 19, 2008
Decision	Substantially Equivalent
Regulation	868.6250

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Source

View the full FDA submission: accessdata.fda.gov

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