Cypress Medical Products Sterile Latex Examination Glove

FDA 510(k) K950254 · Cypress Medical Products, Ltd.

Substantially Equivalent

510(k) numberK950254

Submission

Device name
Cypress Medical Products Sterile Latex Examination Glove
Applicant
Cypress Medical Products, Ltd.
Mc Henry, IL, US
Received
January 23, 1995
Decision date
March 31, 1995
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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K221648Iconic Latex GloveLYY · Traditional Iconic Medicare Sdn Bhd08/25/2022SE

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K952367Cypress Medical Products Vinyl Examination GloveLYY · Traditional 07/05/1995SE
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Questions and answers

When was Cypress Medical Products Sterile Latex Examination Glove cleared by the FDA?

Cypress Medical Products Sterile Latex Examination Glove (K950254) received a 510(k) decision of Substantially Equivalent on March 31, 1995, 67 days after the submission was received.

What is the product code of K950254?

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