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FDA 510(k)

POWERED NITRILE BLUE EXAMINATION GLOVES

K-Number: K061505 · 2007-04-09

ApplicantLiwe Trading
Decision Date2007-04-09
Product CodeLZA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWERED NITRILE BLUE EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Liwe Trading. It received FDA 510(k) clearance on 2007-04-09 under 510(k) number K061505. 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 POWERED NITRILE BLUE EXAMINATION GLOVES?

POWERED NITRILE BLUE EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2007-04-09. The listed applicant is Liwe Trading. The 510(k) number is K061505.

When did POWERED NITRILE BLUE EXAMINATION GLOVES receive FDA 510(k) clearance?

POWERED NITRILE BLUE EXAMINATION GLOVES received FDA 510(k) clearance on 2007-04-09, under 510(k) number K061505.

Who is the listed applicant for POWERED NITRILE BLUE EXAMINATION GLOVES?

The FDA 510(k) record lists Liwe Trading as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWERED NITRILE BLUE EXAMINATION GLOVES?

The FDA product code for POWERED NITRILE BLUE 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 Liwe Trading 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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