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FDA 510(k)

Seaman Pro/Seaman

K-Number: K252228 · 2026-04-09

ApplicantCheckcells, Inc.
Decision Date2026-04-09
Product CodePOV
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

Seaman Pro/Seaman is a medical device manufactured by Checkcells, Inc.. It received FDA 510(k) clearance on 2026-04-09 under approval number K252228. The device is classified under product code POV. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Seaman Pro/Seaman?

Seaman Pro/Seaman is a medical device that received FDA 510(k) clearance on 2026-04-09. It is manufactured by Checkcells, Inc.. The 510(k) number is K252228.

When was Seaman Pro/Seaman approved by the FDA?

Seaman Pro/Seaman received FDA 510(k) clearance on 2026-04-09, under approval number K252228.

What company makes Seaman Pro/Seaman?

Seaman Pro/Seaman is manufactured by Checkcells, Inc..

What is the FDA product code for Seaman Pro/Seaman?

The FDA product code for Seaman Pro/Seaman is POV.

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Official Source

View on FDA Database →

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