Cleared Traditional

K992122 - TRU-TOUCH PF VINYL POWDER FREE EXAMINATION GLOVE

K992122 is an FDA 510(k) clearance for TRU-TOUCH PF VINYL POWDER FREE EXAMINAT..., manufactured by Maxxim Medical. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 22-day FDA review.

K992122 · Maxxim Medical · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 1999
Decision
22d
Days
Class 1
Risk

K992122 is an FDA 510(k) clearance for the TRU-TOUCH PF VINYL POWDER FREE EXAMINATION GLOVE. Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Maxxim Medical (Oldsmar, US). The FDA issued a Cleared decision on July 15, 1999 after a review of 22 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 Maxxim Medical devices

FDA 510(k) Submission Details - K992122

510(k) Number K992122 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1999
Decision Date July 15, 1999
Days to Decision 22 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
107d faster than avg
Panel avg: 129d · This submission: 22d
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 637
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K992122.
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K992206 · Shanghai China Star Corp · Jul 1999
SAFESKIN SYNTHETIC BINYO POWDER-FREE POLYMER COATED EXAMINATION GLOVES (GREEN, WHITE)
K991951 · Safeskin Corp. · Jul 1999
PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES
K992205 · Shanghai China Star Corp · Jul 1999
DISPOSABLE VINYL SYNTHETIC EXAM GLOVES, POWDER FREE
K991457 · Shanghai Palomar Mountain Industries, Inc. · Jul 1999
POWDER FREE VINYL EXAMINATION GLOVES
K983856 · Shijiazhuang Brethern Plastic Co., Ltd. · Jun 1999
POWDERED VINYL EXAMINATION GLOVE
K983893 · Shijiazhuang Brethern Plastic Co., Ltd. · Jun 1999