K-number	K251899
Device name	E Blator
Applicant	New Deantronics Taiwan , Ltd.
Product code	GEI
Device class	Class II
Decision date	Oct 1, 2025
Decision	Substantially Equivalent
Regulation	—

AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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E Blator

Everything you need for a 510(k) submission. Nothing you don't.