SwiftSight-BodyComposition
K-Number: K261612 · 2026-10-01
Device Summary
Frequently Asked Questions
What is the SwiftSight-BodyComposition?
SwiftSight-BodyComposition is a medical device that received FDA 510(k) clearance on 2026-10-01. The listed applicant is Airs Medical, Inc.. The 510(k) number is K261612.
When did SwiftSight-BodyComposition receive FDA 510(k) clearance?
SwiftSight-BodyComposition received FDA 510(k) clearance on 2026-10-01, under 510(k) number K261612.
Who is the listed applicant for SwiftSight-BodyComposition?
The FDA 510(k) record lists Airs Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SwiftSight-BodyComposition?
The FDA product code for SwiftSight-BodyComposition is LNH.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Airs Medical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LNH)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.