Cleared Traditional

K102613 - POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

K102613 is an FDA 510(k) clearance for POWDER-FREE VINYL PATIENT EXAMINATION G..., manufactured by Hebei Favor 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 125-day FDA review.

K102613 · Hebei Favor Plastic Co., Ltd. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jan 2011
Decision
125d
Days
Class 1
Risk

K102613 is an FDA 510(k) clearance for the POWDER-FREE VINYL PATIENT EXAMINATION GLOVES. Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Hebei Favor Plastic Co., Ltd. (Beijing, CN). The FDA issued a Cleared decision on January 13, 2011 after a review of 125 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K102613

510(k) Number K102613 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 10, 2010
Decision Date January 13, 2011
Days to Decision 125 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
4d faster than avg
Panel avg: 129d · This submission: 125d
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 749
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K102613.
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K102085 · Shijiazhuang Glory Plastic Co., Ltd. · Apr 2011
SYNTHETIC VINYL EXAMINATION GLOVE, POWDER FREE
K110224 · Weifang Beihai Color Printing Packagging Co., Ltd. · Mar 2011
VINYL EXAMINATION GLOVE POWDER FREE (CLEAR, NON-COLRED) /YELLOW/WHITE)
K103772 · Advanced Medical Devices Factory · Feb 2011
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K102817 · Hebei Hongtai Plastic Products Co., Ltd. · Dec 2010
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K102819 · Hebei Hongtai Plastic Products Co., Ltd. · Dec 2010
SYNTHETIC, POWDER-FREE NITRILE EXAMINATION
K102593 · Zibo Yinghao Medical Products Co., Ltd. · Dec 2010
K102613 · POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
Download PDF FDA Summary Hebei Favor Plastic C…