Black Nitrile Powder Free Patient Examination Glove, Non Sterile
K-Number: K233740 · 2024-02-13
Device Summary
Frequently Asked Questions
What is the Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
Black Nitrile Powder Free Patient Examination Glove, Non Sterile is a medical device that received FDA 510(k) clearance on 2024-02-13. The listed applicant is W.A. Rubbermate Co., Ltd.. The 510(k) number is K233740.
When did Black Nitrile Powder Free Patient Examination Glove, Non Sterile receive FDA 510(k) clearance?
Black Nitrile Powder Free Patient Examination Glove, Non Sterile received FDA 510(k) clearance on 2024-02-13, under 510(k) number K233740.
Who is the listed applicant for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA 510(k) record lists W.A. Rubbermate Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile?
The FDA product code for Black Nitrile Powder Free Patient Examination Glove, Non Sterile is LZA.
Related Clinical Trials
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.
Related Devices (Code: LZA)
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.
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.