FDA 510(k)

一次性ラテックス検査手袋（非滅菌）、一次性ニトリル検査手袋（非滅菌）

K番号: K203074 · 2021-11-19

決定日2021-11-19

製品コードLYY

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定大幅同等

医療機器の概要

Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile) is the device name listed in this FDA 510(k) record. The listed applicant is Pt. Universal Gloves. It received FDA 510(k) clearance on 2021-11-19 under 510(k) number K203074. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile)?

Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile) is a medical device that received FDA 510(k) clearance on 2021-11-19. The listed applicant is Pt. Universal Gloves. The 510(k) number is K203074.

When did Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile) receive FDA 510(k) clearance?

Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile) received FDA 510(k) clearance on 2021-11-19, under 510(k) number K203074.

Who is the listed applicant for Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile)?

The FDA 510(k) record lists Pt. Universal Gloves as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile)?

The FDA product code for Disposable Latex Examination Gloves (Non-Sterile), Disposable Nitrile Examination Gloves (Non-Sterile) is LYY.

申請者としてPt. Universal Glovesを記載するその他の記録

K211360一次性ニトリル粉を含まない検査手袋（非滅菌）K201576一次性ラテックス粉を含まない検査手袋（非滅菌）

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