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FDA 510(k)

Disposable Extension Set

K-Number: K222766 · 2024-04-12

ApplicantShandong Ande Healthcare Apparatus Co., Ltd.
Decision Date2024-04-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Disposable Extension Set is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Ande Healthcare Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2024-04-12 under 510(k) number K222766. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Extension Set?

Disposable Extension Set is a medical device that received FDA 510(k) clearance on 2024-04-12. The listed applicant is Shandong Ande Healthcare Apparatus Co., Ltd.. The 510(k) number is K222766.

When did Disposable Extension Set receive FDA 510(k) clearance?

Disposable Extension Set received FDA 510(k) clearance on 2024-04-12, under 510(k) number K222766.

Who is the listed applicant for Disposable Extension Set?

The FDA 510(k) record lists Shandong Ande Healthcare Apparatus Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Extension Set?

The FDA product code for Disposable Extension Set is FPA.

Related Devices (Code: FPA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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