K-number	K250766
Device name	LungQ 4
Applicant	Thirona BV
Product code	JAK
Device class	Class II
Decision date	Oct 2, 2025
Decision	Substantially Equivalent
Regulation	892.1750

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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LungQ 4

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