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FDA 510(k)

POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

K-Number: K122396 · 2013-01-31

Decision Date2013-01-31
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) is the device name listed in this FDA 510(k) record. The listed applicant is Wealth on (Jiangsu) Co., Ltd.. It received FDA 510(k) clearance on 2013-01-31 under 510(k) number K122396. 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 POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?

POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) is a medical device that received FDA 510(k) clearance on 2013-01-31. The listed applicant is Wealth on (Jiangsu) Co., Ltd.. The 510(k) number is K122396.

When did POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) receive FDA 510(k) clearance?

POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) received FDA 510(k) clearance on 2013-01-31, under 510(k) number K122396.

Who is the listed applicant for POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?

The FDA 510(k) record lists Wealth on (Jiangsu) Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)?

The FDA product code for POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED) 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 Wealth on (Jiangsu) 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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