Biogel Orthopaedic Surgical Glove with Non-Pryogenic Statement

FDA 510(k) K071465 · Molnlycke Health Care Us, LLC

Substantially Equivalent

510(k) numberK071465

Submission

Device name
Biogel Orthopaedic Surgical Glove with Non-Pryogenic Statement
Applicant
Molnlycke Health Care Us, LLC
Norcross, GA, US
Received
May 29, 2007
Decision date
September 11, 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 Biogel Orthopaedic Surgical Glove with Non-Pryogenic Statement cleared by the FDA?

Biogel Orthopaedic Surgical Glove with Non-Pryogenic Statement (K071465) received a 510(k) decision of Substantially Equivalent on September 11, 2007, 105 days after the submission was received.

What is the product code of K071465?

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