Ultralon Powder Free Latex Surgical Glove

FDA 510(k) K973699 · Johnson & Johnson Medical, Inc.

Substantially Equivalent

510(k) numberK973699

Submission

Device name
Ultralon Powder Free Latex Surgical Glove
Applicant
Johnson & Johnson Medical, Inc.
Arlington, TX, US
Received
September 29, 1997
Decision date
December 16, 1997
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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K240790Polyisoprene Surgical glovesKGO · Traditional Suzhou Colour-Way New Material Co., Ltd.08/23/2024SE
K232079Natural Rubber Latex Surgical Glove, Powder Free, Sterile, Tested for Use with…KGO · Traditional Wrp Asia Pacific Sdn. Bhd.03/28/2024SE
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K231902GAMMEX PI Hybrid Micro (340002055); GAMMEX PI Hybrid Micro (340002060); GAMMEX PI Hybrid…KGO · Traditional Ansell Healthcare10/20/2023SE
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K231446Single-Use Latex Sterile Surgical Gloves (SG100)KGO · Traditional Fitone Latex Products Co., Ltd. Guangdong09/22/2023SE
K230578Polyisoprene Surgical Glove (Unified Double Layer), Sterile, Tested for Use with…KGO · Traditional Wrp Asia Pacific Sdn. Bhd.08/31/2023SE

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Questions and answers

When was Ultralon Powder Free Latex Surgical Glove cleared by the FDA?

Ultralon Powder Free Latex Surgical Glove (K973699) received a 510(k) decision of Substantially Equivalent on December 16, 1997, 78 days after the submission was received.

What is the product code of K973699?

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