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FDA 510(k)

VINYL PATIENT EXAMINATION GLOVE, POWDERED

K-Number: K971423 · 1997-05-23

Decision Date1997-05-23
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VINYL PATIENT EXAMINATION GLOVE, POWDERED is the device name listed in this FDA 510(k) record. The listed applicant is Shanghai Foremost Plastic Industrial Co., Ltd.. It received FDA 510(k) clearance on 1997-05-23 under 510(k) number K971423. 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 PATIENT EXAMINATION GLOVE, POWDERED?

VINYL PATIENT EXAMINATION GLOVE, POWDERED is a medical device that received FDA 510(k) clearance on 1997-05-23. The listed applicant is Shanghai Foremost Plastic Industrial Co., Ltd.. The 510(k) number is K971423.

When did VINYL PATIENT EXAMINATION GLOVE, POWDERED receive FDA 510(k) clearance?

VINYL PATIENT EXAMINATION GLOVE, POWDERED received FDA 510(k) clearance on 1997-05-23, under 510(k) number K971423.

Who is the listed applicant for VINYL PATIENT EXAMINATION GLOVE, POWDERED?

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

What is the FDA product code for VINYL PATIENT EXAMINATION GLOVE, POWDERED?

The FDA product code for VINYL PATIENT EXAMINATION GLOVE, POWDERED 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 Foremost Plastic Industrial 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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