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FDA 510(k)

SnapshotNIR model KD205

K-Number: K240601 · 2024-04-02

ApplicantKent Imaging, Inc.
Decision Date2024-04-02
Product CodeMUD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SnapshotNIR model KD205 is a medical device manufactured by Kent Imaging, Inc.. It received FDA 510(k) clearance on 2024-04-02 under approval number K240601. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SnapshotNIR model KD205?

SnapshotNIR model KD205 is a medical device that received FDA 510(k) clearance on 2024-04-02. It is manufactured by Kent Imaging, Inc.. The 510(k) number is K240601.

When was SnapshotNIR model KD205 approved by the FDA?

SnapshotNIR model KD205 received FDA 510(k) clearance on 2024-04-02, under approval number K240601.

What company makes SnapshotNIR model KD205?

SnapshotNIR model KD205 is manufactured by Kent Imaging, Inc..

What is the FDA product code for SnapshotNIR model KD205?

The FDA product code for SnapshotNIR model KD205 is MUD.

Other Devices by Kent Imaging, Inc.

K163070Kent Camera K242669SnapshotGLO (KB100)

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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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