FDA 510(k)

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

K-Number: K102444 · 2010-11-22

ApplicantZibo Yingbo Medical Products, Inc.

Decision Date2010-11-22

Product CodeLYZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Zibo Yingbo Medical Products, Inc.. It received FDA 510(k) clearance on 2010-11-22 under 510(k) number K102444. 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 VINYL PATIENT EXAMINATION GLOVES?

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 2010-11-22. The listed applicant is Zibo Yingbo Medical Products, Inc.. The 510(k) number is K102444.

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

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 2010-11-22, under 510(k) number K102444.

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

The FDA 510(k) record lists Zibo Yingbo Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for POWDER-FREE VINYL PATIENT EXAMINATION GLOVES is LYZ.

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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.