Uniseal Gloves (Low Protein,Powder Free)

FDA 510(k) K963211 · American Healthcare Products, Inc.

Substantially Equivalent

510(k) numberK963211

Submission

Device name
Uniseal Gloves (Low Protein,Powder Free)
Applicant
American Healthcare Products, Inc.
Encino, CA, US
Received
August 16, 1996
Decision date
November 22, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
LYY – Latex Patient Examination Glove
Device class
Class I (low risk)
Regulation
21 CFR 880.6250
Specialty
General Hospital

A latex patient examination glove is a disposable device made of natural rubber latex that may or may not bear a trace amount of residual powder, and is intended to be worn on the hand for medical purposes to provide a barrier against potentially infectious materials and other contaminants.

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Questions and answers

When was Uniseal Gloves (Low Protein,Powder Free) cleared by the FDA?

Uniseal Gloves (Low Protein,Powder Free) (K963211) received a 510(k) decision of Substantially Equivalent on November 22, 1996, 98 days after the submission was received.

What is the product code of K963211?

The FDA product code is LYY – Latex Patient Examination Glove, a Class I (low risk) device regulated under 21 CFR 880.6250.