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FDA 510(k)

Intermittent nelaton catheter for single use

K-Number: K222677 · 2023-04-05

ApplicantHangzhou Jimushi Meditech Co., Ltd.
Decision Date2023-04-05
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Intermittent nelaton catheter for single use is a medical device manufactured by Hangzhou Jimushi Meditech Co., Ltd.. It received FDA 510(k) clearance on 2023-04-05 under approval number K222677. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intermittent nelaton catheter for single use?

Intermittent nelaton catheter for single use is a medical device that received FDA 510(k) clearance on 2023-04-05. It is manufactured by Hangzhou Jimushi Meditech Co., Ltd.. The 510(k) number is K222677.

When was Intermittent nelaton catheter for single use approved by the FDA?

Intermittent nelaton catheter for single use received FDA 510(k) clearance on 2023-04-05, under approval number K222677.

What company makes Intermittent nelaton catheter for single use?

Intermittent nelaton catheter for single use is manufactured by Hangzhou Jimushi Meditech Co., Ltd..

What is the FDA product code for Intermittent nelaton catheter for single use?

The FDA product code for Intermittent nelaton catheter for single use is EZD.

Related Clinical Trials

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Other Devices by Hangzhou Jimushi Meditech Co., Ltd.

K200134Jimushi Sterile Urethral Catheter for single use

Related Devices (Code: EZD)

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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.

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