Zimmer Cut Resistant Glove Liner, Xsmall, Small, Medium, Large, Xlarge

FDA 510(k) K063582 · Zimmer, Inc.

Substantially Equivalent

510(k) numberK063582

Submission

Device name
Zimmer Cut Resistant Glove Liner, Xsmall, Small, Medium, Large, Xlarge
Applicant
Zimmer, Inc.
Dover, OH, US
Received
December 1, 2006
Decision date
April 26, 2007
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KGO – Surgeon'S Gloves
Device class
Class I (low risk)
Regulation
21 CFR 878.4460
Specialty
General, Plastic Surgery

A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a barrier against potentially infectious materials and other contaminants.

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Questions and answers

When was Zimmer Cut Resistant Glove Liner, Xsmall, Small, Medium, Large, Xlarge cleared by the FDA?

Zimmer Cut Resistant Glove Liner, Xsmall, Small, Medium, Large, Xlarge (K063582) received a 510(k) decision of Substantially Equivalent on April 26, 2007, 146 days after the submission was received.

What is the product code of K063582?

The FDA product code is KGO – Surgeon'S Gloves, a Class I (low risk) device regulated under 21 CFR 878.4460.