FDA 510(k)

Crossloop

K-Number: K241962 · 2025-03-27

Decision Date2025-03-27

Product CodeDQX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

Crossloop is a medical device manufactured by Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2025-03-27 under approval number K241962. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Crossloop?

Crossloop is a medical device that received FDA 510(k) clearance on 2025-03-27. It is manufactured by Asahi Intecc Co., Ltd.. The 510(k) number is K241962.

When was Crossloop approved by the FDA?

Crossloop received FDA 510(k) clearance on 2025-03-27, under approval number K241962.

What company makes Crossloop?

Crossloop is manufactured by Asahi Intecc Co., Ltd..

What is the FDA product code for Crossloop?

The FDA product code for Crossloop is DQX.

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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.