Cleared Traditional

K100855 - POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

K100855 is an FDA 510(k) clearance for POWDER FREE VINYL PATIENT EXAMINATION G..., manufactured by Suzhou Shengyuda Plastic Products Co., Ltd.. The device is a Class 1 General Hospital device with product code LYZ cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K100855 · Suzhou Shengyuda Plastic Products Co., Ltd. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Apr 2010
Decision
27d
Days
Class 1
Risk

K100855 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 Suzhou Shengyuda Plastic Products Co., Ltd. (Beijing, CN). The FDA issued a Cleared decision on April 22, 2010 after a review of 27 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 - K100855

510(k) Number K100855 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 2010
Decision Date April 22, 2010
Days to Decision 27 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
102d faster than avg
Panel avg: 129d · This submission: 27d
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 K100855.
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, YELLOW COLOR
K100486 · Zibo Yinghao Medical Products Co., Ltd. · May 2010
STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE
K093263 · Qingdao Lang Hui Import & Export Co., Ltd. · Apr 2010
POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
K100733 · Rayen Safety Products Limited · Apr 2010
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K100392 · Tangshan Jiaxing Plastic Products Co., LT · Apr 2010
POWDER-FREE VINYL EXAM GLOVES
K091772 · Shijiazhuang Huijingyuan Plastic Co, Ltd. · Apr 2010
VINYL PATIENT EXAM GLOVES PRE-POWERED, CLEAR
K091770 · Shijiazhuang Huijingyuan Plastic Co, Ltd. · Apr 2010
K100855 · POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
Download PDF FDA Summary Suzhou Shengyuda Plas…