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FDA 510(k)

RG 3ml Medication Cartridge

K-Number: K201634 · 2021-03-26

ApplicantChengdu Shifeng Medical Technology Co., Ltd.
Decision Date2021-03-26
Product CodeMRZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RG 3ml Medication Cartridge is the device name listed in this FDA 510(k) record. The listed applicant is Chengdu Shifeng Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-03-26 under 510(k) number K201634. The device is classified under product code MRZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RG 3ml Medication Cartridge?

RG 3ml Medication Cartridge is a medical device that received FDA 510(k) clearance on 2021-03-26. The listed applicant is Chengdu Shifeng Medical Technology Co., Ltd.. The 510(k) number is K201634.

When did RG 3ml Medication Cartridge receive FDA 510(k) clearance?

RG 3ml Medication Cartridge received FDA 510(k) clearance on 2021-03-26, under 510(k) number K201634.

Who is the listed applicant for RG 3ml Medication Cartridge?

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

What is the FDA product code for RG 3ml Medication Cartridge?

The FDA product code for RG 3ml Medication Cartridge is MRZ.

Related Devices (Code: MRZ)

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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