NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES
K-Number: K072400 · 2008-03-27
Advertisement
Device Summary
Frequently Asked Questions
What is the NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES?
NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2008-03-27. The listed applicant is Sgmp Co., Ltd.. The 510(k) number is K072400.
When did NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?
NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2008-03-27, under 510(k) number K072400.
Who is the listed applicant for NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES?
The FDA 510(k) record lists Sgmp Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES?
The FDA product code for NON-STERILE, POWDER-FREE, BLACK NITRILE EXAMINATION GLOVES 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 Sgmp Co., Ltd. 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.
Advertisement