meddevicedb.com FDA Device Reference

SwiftSight-BodyComposition

K261612 Class II Traditional
Decision Date
2026-10-01
Sponsor / Applicant
Airs Medical, Inc.

Technical Specification

510(k) Submission ID K261612
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2026-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SwiftSight-BodyComposition received FDA 510(k) clearance under submission number K261612, sponsored by Airs Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.