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FDA 510(k)

POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES

K-Number: K092000 · 2009-09-18

Decision Date2009-09-18
Product CodeLYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Shangdong Zibo Shanchuan Medical Instruments Co.. It received FDA 510(k) clearance on 2009-09-18 under 510(k) number K092000. 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 POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES?

POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2009-09-18. The listed applicant is Shangdong Zibo Shanchuan Medical Instruments Co.. The 510(k) number is K092000.

When did POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?

POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2009-09-18, under 510(k) number K092000.

Who is the listed applicant for POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES?

The FDA 510(k) record lists Shangdong Zibo Shanchuan Medical Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POWDER-FREE, YELLOW VINYL PATIENT EXAMINATION GLOVES?

The FDA product code for POWDER-FREE, YELLOW VINYL 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 Shangdong Zibo Shanchuan Medical Instruments Co. 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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