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FDA 510(k)

Bone Marrow Biopsy Needle

K-Number: K242322 · 2025-01-24

Decision Date2025-01-24
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Bone Marrow Biopsy Needle is a medical device manufactured by Zhejiang Curaway Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-01-24 under approval number K242322. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bone Marrow Biopsy Needle?

Bone Marrow Biopsy Needle is a medical device that received FDA 510(k) clearance on 2025-01-24. It is manufactured by Zhejiang Curaway Medical Technology Co., Ltd.. The 510(k) number is K242322.

When was Bone Marrow Biopsy Needle approved by the FDA?

Bone Marrow Biopsy Needle received FDA 510(k) clearance on 2025-01-24, under approval number K242322.

What company makes Bone Marrow Biopsy Needle?

Bone Marrow Biopsy Needle is manufactured by Zhejiang Curaway Medical Technology Co., Ltd..

What is the FDA product code for Bone Marrow Biopsy Needle?

The FDA product code for Bone Marrow Biopsy Needle is KNW.

Related Clinical Trials

Other Devices by Zhejiang Curaway Medical Technology Co., Ltd.

Related Devices (Code: KNW)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.