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FDA 510(k)

NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES

K-Number: K000868 · 2000-04-20

Decision Date2000-04-20
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Sgmp Co., Ltd.. It received FDA 510(k) clearance on 2000-04-20 under 510(k) number K000868. 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 NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES?

NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2000-04-20. The listed applicant is Sgmp Co., Ltd.. The 510(k) number is K000868.

When did NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES receive FDA 510(k) clearance?

NON-STERILE POWDER-FREE, BLUE NITRILE EXAMINATION GLOVES received FDA 510(k) clearance on 2000-04-20, under 510(k) number K000868.

Who is the listed applicant for NON-STERILE POWDER-FREE, BLUE 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, BLUE NITRILE EXAMINATION GLOVES?

The FDA product code for NON-STERILE POWDER-FREE, BLUE 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.

View all 31 devices →

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.

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