Nitrile Examination Gloves
K-Number: K222813 · 2023-03-16
Decision Date2023-03-16
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Nitrile Examination Gloves is a medical device manufactured by Ecoglove Medical Manufacturing Company Limited. It received FDA 510(k) clearance on 2023-03-16 under approval number K222813. The device is classified under product code LZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nitrile Examination Gloves?
Nitrile Examination Gloves is a medical device that received FDA 510(k) clearance on 2023-03-16. It is manufactured by Ecoglove Medical Manufacturing Company Limited. The 510(k) number is K222813.
When was Nitrile Examination Gloves approved by the FDA?
Nitrile Examination Gloves received FDA 510(k) clearance on 2023-03-16, under approval number K222813.
What company makes Nitrile Examination Gloves?
Nitrile Examination Gloves is manufactured by Ecoglove Medical Manufacturing Company Limited.
What is the FDA product code for Nitrile Examination Gloves?
The FDA product code for Nitrile Examination Gloves is LZA.
Related Clinical Trials
Related Devices (Code: LZA)
K161215Brightway Brand Nitrile Examination Gloves, Powder Free, [Sterling/Grey] Tested For Use With Chemotherapy DrugsBrightway Holdings Sdn. Bhd.
K161932Powder Free Polychloroprene Examination Glove Blue, Powder Free Polychloroprene Examination Glove PinkTerang Nusa Sdn Bhd
K161944Synthetic Nitrile Patient Examination Gloves, Powder Free, Blue Color, and Tested for Use with Chemotherapy DrugsShandong Baisheng Medical Products Co., Ltd.
K161074Powder Free Nitrile Examination Gloves Flock-Lined, Black ColorShen Wei (Usa), Inc.
K162113Powder Free Nitrile Examination Gloves (Blue)Nam Viet Glove Joint Stock Company
K162095Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use with Chemotherapy Drugs (Original Blue, Cobalt Blue)Yty Industry (Manjung) Sdn Bhd
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.