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FDA 510(k)

Easycess Aspiration Pump

K-Number: K233428 · 2023-11-03

Decision Date2023-11-03
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Easycess Aspiration Pump is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Easycess Medical Co.,Ltd. It received FDA 510(k) clearance on 2023-11-03 under 510(k) number K233428. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Easycess Aspiration Pump?

Easycess Aspiration Pump is a medical device that received FDA 510(k) clearance on 2023-11-03. The listed applicant is Guangzhou Easycess Medical Co.,Ltd. The 510(k) number is K233428.

When did Easycess Aspiration Pump receive FDA 510(k) clearance?

Easycess Aspiration Pump received FDA 510(k) clearance on 2023-11-03, under 510(k) number K233428.

Who is the listed applicant for Easycess Aspiration Pump?

The FDA 510(k) record lists Guangzhou Easycess Medical Co.,Ltd as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Easycess Aspiration Pump?

The FDA product code for Easycess Aspiration Pump is JCX.

Other records listing Guangzhou Easycess Medical Co.,Ltd as applicant

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.

Related Devices (Code: JCX)

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.

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.