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FDA 510(k)

SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES

K-Number: K000166 · 2000-02-22

Decision Date2000-02-22
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shijiazhuang Great Eagle Plastic Products Co., Ltd.. It received FDA 510(k) clearance on 2000-02-22 under 510(k) number K000166. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES?

SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2000-02-22. The listed applicant is Shijiazhuang Great Eagle Plastic Products Co., Ltd.. The 510(k) number is K000166.

When did SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2000-02-22, under 510(k) number K000166.

Who is the listed applicant for SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES?

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

What is the FDA product code for SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES?

The FDA product code for SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES is LYZ.

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 Shijiazhuang Great Eagle Plastic Products 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: LYZ)

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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