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FDA 510(k)

Jimushi Sterile Urethral Catheter for single use

K-Number: K200134 · 2020-06-01

ApplicantHangzhou Jimushi Meditech Co., Ltd.
Decision Date2020-06-01
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Jimushi Sterile Urethral Catheter for single use is a medical device manufactured by Hangzhou Jimushi Meditech Co., Ltd.. It received FDA 510(k) clearance on 2020-06-01 under approval number K200134. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Jimushi Sterile Urethral Catheter for single use?

Jimushi Sterile Urethral Catheter for single use is a medical device that received FDA 510(k) clearance on 2020-06-01. It is manufactured by Hangzhou Jimushi Meditech Co., Ltd.. The 510(k) number is K200134.

When was Jimushi Sterile Urethral Catheter for single use approved by the FDA?

Jimushi Sterile Urethral Catheter for single use received FDA 510(k) clearance on 2020-06-01, under approval number K200134.

What company makes Jimushi Sterile Urethral Catheter for single use?

Jimushi Sterile Urethral Catheter for single use is manufactured by Hangzhou Jimushi Meditech Co., Ltd..

What is the FDA product code for Jimushi Sterile Urethral Catheter for single use?

The FDA product code for Jimushi Sterile Urethral Catheter for single use is GBM.

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Other Devices by Hangzhou Jimushi Meditech Co., Ltd.

K222677Intermittent nelaton catheter for single use

Related Devices (Code: GBM)

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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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