Female Culture Device; Male Culture Device; Transfer Device; Access Dev… - FDA 510(k) K252899

医療機器の概要

Female Culture Device; Male Culture Device; Transfer Device; Access Device is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Kindly Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2026-06-02 under 510(k) number K252899. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Female Culture Device; Male Culture Device; Transfer Device; Access Device?

Female Culture Device; Male Culture Device; Transfer Device; Access Device is a medical device that received FDA 510(k) clearance on 2026-06-02. The listed applicant is Zhejiang Kindly Medical Device Co., Ltd.. The 510(k) number is K252899.

When did Female Culture Device; Male Culture Device; Transfer Device; Access Device receive FDA 510(k) clearance?

Female Culture Device; Male Culture Device; Transfer Device; Access Device received FDA 510(k) clearance on 2026-06-02, under 510(k) number K252899.

Who is the listed applicant for Female Culture Device; Male Culture Device; Transfer Device; Access Device?

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

What is the FDA product code for Female Culture Device; Male Culture Device; Transfer Device; Access Device?

The FDA product code for Female Culture Device; Male Culture Device; Transfer Device; Access Device is JKA.

申請者としてZhejiang Kindly Medical Device Co., Ltd.を記載するその他の記録

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K233037Sterile Hypodermic Needles for Single Use

関連機器（コード：JKA）

関連レコードは、名称、製品コード、その他のメタデータを使用して自動的にマッチングされます。マッチは検証された臨床的、科学的、企業的、または規制上の関係を確立するものではありません。リンクされた公式情報源をご確認ください。

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