K-number	K252330
Device name	DeepRESP
Applicant	Nox Medical Ehf
Product code	OLZ
Device class	Class II
Decision date	Nov 17, 2025
Decision	Substantially Equivalent
Regulation	882.1400

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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DeepRESP

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