Cleared Traditional

K892574 - VINYL PATIENT EXAMINATION GLOVES

K892574 is an FDA 510(k) clearance for VINYL PATIENT EXAMINATION GLOVES, manufactured by Encore Products, Inc.. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 53-day FDA review.

K892574 · Encore Products, Inc. · General Hospital
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Jun 1989
Decision
53d
Days
Class 1
Risk

K892574 is an FDA 510(k) clearance for the VINYL PATIENT EXAMINATION GLOVES. Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Encore Products, Inc. (Hauppauge, US). The FDA issued a Cleared decision on June 2, 1989 after a review of 53 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6250 - the FDA general hospital device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Encore Products, Inc. devices

FDA 510(k) Submission Details - K892574

510(k) Number K892574 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 10, 1989
Decision Date June 02, 1989
Days to Decision 53 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
76d faster than avg
Panel avg: 129d · This submission: 53d
Pathway characteristics
Predicate-based equivalence.

LYZ Device Classification - Class 1, General Controls

Product Code LYZ Vinyl Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Vinyl Patient Examination Glove Is A Disposable Device Made Of Poly(vinyl Chloride) 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.
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - LYZ Vinyl Patient Examination Glove

All 615
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K892574.
PREPOWDERED VINYL EXAM GLOVES
K893334 · Dynarex Corp. · Aug 1989
TRU-TOUCH VINYL EXAM GLOVES (BELGIUM)
K891948 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jul 1989
TRU-TOUCH VINYL EXAM GLOVES (CANADA)
K891952 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Jun 1989
PATIENT EXAMINATION GLOVES (VINYL)
K891717 · Ulti-Med Intl., Inc. · May 1989
PATIENT EXAMINATION GLOVES (VINYL)
K891941 · Cypress Medical Products, Ltd. · May 1989
PATIENT EXAMINATION GLOVES (VINYL)
K891860 · Cypress Medical Products, Ltd. · Apr 1989