Cleared Traditional

K992922 - SENSI-PRO, DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR

K992922 is an FDA 510(k) clearance for SENSI-PRO, manufactured by Shijiazhuang Hongray 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 37-day FDA review.

K992922 · Shijiazhuang Hongray Plastic Products Co., Ltd. · General Hospital
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Oct 1999
Decision
37d
Days
Class 1
Risk

K992922 is an FDA 510(k) clearance for the SENSI-PRO, DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR. Classified as Vinyl Patient Examination Glove (product code LYZ), Class I - General Controls.

Submitted by Shijiazhuang Hongray Plastic Products Co., Ltd. (Shijiazhuang, CN). The FDA issued a Cleared decision on October 6, 1999 after a review of 37 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 Shijiazhuang Hongray Plastic Products Co., Ltd. devices

FDA 510(k) Submission Details - K992922

510(k) Number K992922 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 1999
Decision Date October 06, 1999
Days to Decision 37 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
92d faster than avg
Panel avg: 129d · This submission: 37d
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 205
Devices cleared under the same product code (LYZ) and FDA review panel - the closest regulatory comparables to K992922.
SYNTHETIC POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K992555 · Shijiazhuang Great Vision Plastic Products Co., LT · Oct 1999
SENSICARE XP VINYL POWDER FREE MEDICAL EXAMINATION GLOVE
K992865 · Maxxim Medical · Oct 1999
SYNTHETIC POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION GLOVES
K992861 · Shijiazhuang Great Eagle Plastic Products Co., Ltd. · Oct 1999
PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES
K992271 · Shanghai Cosmos Corp. · Oct 1999
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K992272 · Shanghai Cosmos Corp. · Oct 1999
DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR
K992860 · Shijiazhuang Hongray Plastic Products Co., Ltd. · Sep 1999