FDA 510(k)

Swift Ray 1

K-Number: K251678 · 2026-02-24

Decision Date2026-02-24

Product CodeQJF

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

Swift Ray 1 is the device name listed in this FDA 510(k) record. The listed applicant is Swift Medical, Inc.. It received FDA 510(k) clearance on 2026-02-24 under 510(k) number K251678. The device is classified under product code QJF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Swift Ray 1?

Swift Ray 1 is a medical device that received FDA 510(k) clearance on 2026-02-24. The listed applicant is Swift Medical, Inc.. The 510(k) number is K251678.

When did Swift Ray 1 receive FDA 510(k) clearance?

Swift Ray 1 received FDA 510(k) clearance on 2026-02-24, under 510(k) number K251678.

Who is the listed applicant for Swift Ray 1?

The FDA 510(k) record lists Swift Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Swift Ray 1?

The FDA product code for Swift Ray 1 is QJF.

Related Devices (Code: QJF)

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.

K242669SnapshotGLO (KB100)Kent Imaging, Inc.K230734Multispectral Imager Kit (MSI Kit) (300-00015), Multispectral Imager (MSI) (300-00009)Precision Healing, LLC K213840MolecuLight I:XMolecuLight, Inc.K211901MolecuLightDXMolecuLight, Inc.K210882MolecuLight I:XMolecuLight, Inc.K191371MolecuLight i:XMolecuLight, Inc.

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.