Cleared Traditional

K122893 - POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)

K122893 is an FDA 510(k) clearance for POWDER-FREE VINYL PATIENT EXAMINATION G..., manufactured by Geenli Plastic Co, Ltd.. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K122893 · Geenli Plastic Co, Ltd. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2012
Decision
71d
Days
Class 1
Risk

K122893 is an FDA 510(k) clearance for the POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED). Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Geenli Plastic Co, Ltd. (Beijing, CN). The FDA issued a Cleared decision on November 30, 2012 after a review of 71 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.

FDA 510(k) Submission Details - K122893

510(k) Number K122893 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 20, 2012
Decision Date November 30, 2012
Days to Decision 71 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
58d faster than avg
Panel avg: 129d · This submission: 71d
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 741
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K122893.
POWERED VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K122396 · Wealth on (Jiangsu) Co., Ltd. · Jan 2013
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)
K122828 · Shandong Hongxin Chemicals Co., Ltd. · Dec 2012
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)
K122835 · Yuanhang Plastic Co., Ltd. · Dec 2012
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)
K122920 · Hebei Leader Plastic Co., Ltd. · Nov 2012
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K122266 · Shandong Junfeng Industries Co., Ltd. · Sep 2012
POWER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)
K120968 · Tangshan Zhonghong Pulin Plastic Co.,Ltd · Sep 2012
K122893 · POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR(NON-COLORED)
Download PDF FDA Summary Geenli Plastic Co, Lt…