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FDA 510(k)

VINYL EXAMINATION GLOVES

K-Number: K930266 · 1993-11-22

Decision Date1993-11-22
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai PM Plastics Enterise Co., Ltd.. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K930266. 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 VINYL EXAMINATION GLOVES?

VINYL EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is Shanghai PM Plastics Enterise Co., Ltd.. The 510(k) number is K930266.

When did VINYL EXAMINATION GLOVES receive FDA 510(k) clearance?

VINYL EXAMINATION GLOVES received FDA 510(k) clearance on 1993-11-22, under 510(k) number K930266.

Who is the listed applicant for VINYL EXAMINATION GLOVES?

The FDA 510(k) record lists Shanghai PM Plastics Enterise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VINYL EXAMINATION GLOVES?

The FDA product code for VINYL 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 Shanghai PM Plastics Enterise 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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