FDA 510(k)

POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES

K-Number: K021506 · 2002-06-06

ApplicantShijiazhuang Great Vision Plastic Products Co., LT

Decision Date2002-06-06

Product CodeLZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shijiazhuang Great Vision Plastic Products Co., LT. It received FDA 510(k) clearance on 2002-06-06 under 510(k) number K021506. 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 POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES?

POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2002-06-06. The listed applicant is Shijiazhuang Great Vision Plastic Products Co., LT. The 510(k) number is K021506.

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

POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2002-06-06, under 510(k) number K021506.

Who is the listed applicant for POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Shijiazhuang Great Vision Plastic Products Co., LT as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES?

The FDA product code for POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES is LZA.

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Other records listing Shijiazhuang Great Vision Plastic Products Co., LT as applicant

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Related Devices (Code: LZA)

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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.