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FDA 510(k)

Endoscopic Water Pump

K-Number: K241704 · 2025-03-20

Decision Date2025-03-20
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Endoscopic Water Pump is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou AGS MedTech Co., Ltd.. It received FDA 510(k) clearance on 2025-03-20 under 510(k) number K241704. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Endoscopic Water Pump?

Endoscopic Water Pump is a medical device that received FDA 510(k) clearance on 2025-03-20. The listed applicant is Hangzhou AGS MedTech Co., Ltd.. The 510(k) number is K241704.

When did Endoscopic Water Pump receive FDA 510(k) clearance?

Endoscopic Water Pump received FDA 510(k) clearance on 2025-03-20, under 510(k) number K241704.

Who is the listed applicant for Endoscopic Water Pump?

The FDA 510(k) record lists Hangzhou AGS MedTech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Endoscopic Water Pump?

The FDA product code for Endoscopic Water Pump is OCX.

Other records listing Hangzhou AGS MedTech 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.

View all 19 devices →

Related Devices (Code: OCX)

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

View on FDA Database →

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