FDA 510(k)

SnapshotGLO (KB100)

K-Number: K242669 · 2025-03-26

Decision Date2025-03-26

Product CodeQJF

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SnapshotGLO (KB100) is the device name listed in this FDA 510(k) record. The listed applicant is Kent Imaging, Inc.. It received FDA 510(k) clearance on 2025-03-26 under 510(k) number K242669. 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 SnapshotGLO (KB100)?

SnapshotGLO (KB100) is a medical device that received FDA 510(k) clearance on 2025-03-26. The listed applicant is Kent Imaging, Inc.. The 510(k) number is K242669.

When did SnapshotGLO (KB100) receive FDA 510(k) clearance?

SnapshotGLO (KB100) received FDA 510(k) clearance on 2025-03-26, under 510(k) number K242669.

Who is the listed applicant for SnapshotGLO (KB100)?

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

What is the FDA product code for SnapshotGLO (KB100)?

The FDA product code for SnapshotGLO (KB100) is QJF.

Other records listing Kent Imaging, 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.

K240601SnapshotNIR model KD205 K201976SnapshotNIR K163070Kent Camera

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.