FDA 510(k)

Sterile Aesthetic Cannula and Hypodermic Needle

Número K: K223327 · 2023-02-16

RequerenteShanghai Kindly Enterprise Development Group Co., Ltd.

Data da decisão2023-02-16

Código do produtoFMI

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

Sterile Aesthetic Cannula and Hypodermic Needle is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Kindly Enterprise Development Group Co., Ltd.. It received FDA 510(k) clearance on 2023-02-16 under 510(k) number K223327. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Sterile Aesthetic Cannula and Hypodermic Needle?

Sterile Aesthetic Cannula and Hypodermic Needle is a medical device that received FDA 510(k) clearance on 2023-02-16. The listed applicant is Shanghai Kindly Enterprise Development Group Co., Ltd.. The 510(k) number is K223327.

When did Sterile Aesthetic Cannula and Hypodermic Needle receive FDA 510(k) clearance?

Sterile Aesthetic Cannula and Hypodermic Needle received FDA 510(k) clearance on 2023-02-16, under 510(k) number K223327.

Who is the listed applicant for Sterile Aesthetic Cannula and Hypodermic Needle?

The FDA 510(k) record lists Shanghai Kindly Enterprise Development Group Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterile Aesthetic Cannula and Hypodermic Needle?

The FDA product code for Sterile Aesthetic Cannula and Hypodermic Needle is FMI.

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