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FDA 510(k)

SnapshotGLO (KB100)

K-Number: K242669 · 2025-03-26

ApplicantKent Imaging, Inc.
Decision Date2025-03-26
Product CodeQJF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SnapshotGLO (KB100) is a medical device manufactured by Kent Imaging, Inc.. It received FDA 510(k) clearance on 2025-03-26 under approval 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. It is manufactured by Kent Imaging, Inc.. The 510(k) number is K242669.

When was SnapshotGLO (KB100) approved by the FDA?

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

What company makes SnapshotGLO (KB100)?

SnapshotGLO (KB100) is manufactured by Kent Imaging, Inc..

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

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

Other Devices by Kent Imaging, Inc.

K163070Kent Camera K240601SnapshotNIR model KD205

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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.

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