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FDA 510(k)

Voyager DSLT (430840610)

K-Number: K252979 · 2026-04-07

ApplicantBelkin Vision, Ltd.
Decision Date2026-04-07
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

Voyager DSLT (430840610) is a medical device manufactured by Belkin Vision, Ltd.. It received FDA 510(k) clearance on 2026-04-07 under approval number K252979. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Voyager DSLT (430840610)?

Voyager DSLT (430840610) is a medical device that received FDA 510(k) clearance on 2026-04-07. It is manufactured by Belkin Vision, Ltd.. The 510(k) number is K252979.

When was Voyager DSLT (430840610) approved by the FDA?

Voyager DSLT (430840610) received FDA 510(k) clearance on 2026-04-07, under approval number K252979.

What company makes Voyager DSLT (430840610)?

Voyager DSLT (430840610) is manufactured by Belkin Vision, Ltd..

What is the FDA product code for Voyager DSLT (430840610)?

The FDA product code for Voyager DSLT (430840610) is HQF.

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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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