Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color
K-Number: K210388 · 2021-12-13
Device Summary
Frequently Asked Questions
What is the Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color?
Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color is a medical device that received FDA 510(k) clearance on 2021-12-13. The listed applicant is Mexpo International, Inc.. The 510(k) number is K210388.
When did Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color receive FDA 510(k) clearance?
Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color received FDA 510(k) clearance on 2021-12-13, under 510(k) number K210388.
Who is the listed applicant for Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color?
The FDA 510(k) record lists Mexpo International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color?
The FDA product code for Non Sterile Nitrile Powder Free Examination Gloves – Blue, Green and Black color 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.
Other records listing Mexpo International, Inc. as applicant
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.