Resist(Tm) Orthopaedic Surgical Glove

FDA 510(k) K913893 · Depuy, Inc.

Substantially Equivalent

510(k) numberK913893

Submission

Device name
Resist(Tm) Orthopaedic Surgical Glove
Applicant
Depuy, Inc.
Warsaw, IN, US
Received
August 30, 1991
Decision date
October 23, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Resist(Tm) Orthopaedic Surgical Glove cleared by the FDA?

Resist(Tm) Orthopaedic Surgical Glove (K913893) received a 510(k) decision of Substantially Equivalent on October 23, 1992, 420 days after the submission was received.

What is the product code of K913893?

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