FDA 510(k)

TOPTOUCH /OTHER CLIENTS PRIVATE LABELING

K-Number: K131826 · 2013-11-22

ApplicantJiangsu Toptouch Glove Co., Ltd.

Decision Date2013-11-22

Product CodeLYZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

TOPTOUCH /OTHER CLIENTS PRIVATE LABELING is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Toptouch Glove Co., Ltd.. It received FDA 510(k) clearance on 2013-11-22 under 510(k) number K131826. 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 TOPTOUCH /OTHER CLIENTS PRIVATE LABELING?

TOPTOUCH /OTHER CLIENTS PRIVATE LABELING is a medical device that received FDA 510(k) clearance on 2013-11-22. The listed applicant is Jiangsu Toptouch Glove Co., Ltd.. The 510(k) number is K131826.

When did TOPTOUCH /OTHER CLIENTS PRIVATE LABELING receive FDA 510(k) clearance?

TOPTOUCH /OTHER CLIENTS PRIVATE LABELING received FDA 510(k) clearance on 2013-11-22, under 510(k) number K131826.

Who is the listed applicant for TOPTOUCH /OTHER CLIENTS PRIVATE LABELING?

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

What is the FDA product code for TOPTOUCH /OTHER CLIENTS PRIVATE LABELING?

The FDA product code for TOPTOUCH /OTHER CLIENTS PRIVATE LABELING 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.