K-number	K253323
Device name	Protrieve Sheath
Applicant	Inari Medical
Product code	QEW
Device class	Class II
Decision date	Oct 29, 2025
Decision	Substantially Equivalent
Regulation	870.5150

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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Protrieve Sheath

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