Cleared Traditional

K951018 - LATEX PATIENT EXAMINATION GLOVE POWDERFREE LAMINATED COPOLYMER

K951018 is an FDA 510(k) clearance for LATEX PATIENT EXAMINATION GLOVE POWDERF..., manufactured by Siam Sempermed Corp., Ltd.. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 175-day FDA review.

K951018 · Siam Sempermed Corp., Ltd. · General Hospital
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Aug 1995
Decision
175d
Days
Class 1
Risk

K951018 is an FDA 510(k) clearance for the LATEX PATIENT EXAMINATION GLOVE POWDERFREE LAMINATED COPOLYMER. Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Siam Sempermed Corp., Ltd. (Hatyai, Songkhla, TH). The FDA issued a Cleared decision on August 28, 1995 after a review of 175 days - an extended review 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: 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.

View all Siam Sempermed Corp., Ltd. devices

FDA 510(k) Submission Details - K951018

510(k) Number K951018 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 06, 1995
Decision Date August 28, 1995
Days to Decision 175 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
46d slower than avg
Panel avg: 129d · This submission: 175d
Pathway characteristics
Predicate-based equivalence.

LYY Device Classification - Class 1, General Controls

Product Code LYY Latex Patient Examination Glove
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6250
Definition A Latex Patient Examination Glove Is A Disposable Device Made Of Natural Rubber Latex 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 - LYY Latex Patient Examination Glove

All 402
Devices cleared under the same product code (LYY) and FDA review panel - the closest regulatory comparables to K951018.
LATEX PATIENT EXAMINATION GLOVE (POWDERFREE/HYPOALLERGENIC) (MODIFICATION)
K954880 · Siam Sempermed Corp., Ltd. · Nov 1995
HYPOALLERGENIC POWDERED AMBIDEXTROUS COAGULATN DIPPED LATEX EXAMINATION GLOVE
K953379 · Ansell, Inc. · Sep 1995
ROYAL SHIELD NON-STERILE POWDER-FREE HYPOALLERGENIC LATEX EXAMINATION GLOVES
K953496 · Shield Gloves Manufacturer (M) Sdn Bhd · Sep 1995
ROYAL SHIELD PINK & BLUE COLORED NON-STERILE LATEX EXAMINATION GLOVES
K952589 · Shield Gloves Manufacturer (M) Sdn Bhd · Aug 1995
SAFESKIN
K952793 · Safeskin Corp. · Aug 1995
SAFESKIN
K952851 · Safeskin Corp. · Aug 1995