Cleared Traditional

K970977 - LATEX EXAMINATION GLOVES, POWDER FREE

K970977 is an FDA 510(k) clearance for LATEX EXAMINATION GLOVES, manufactured by Arista Medi Prima. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 105-day FDA review.

K970977 · Arista Medi Prima · General Hospital
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Jun 1997
Decision
105d
Days
Class 1
Risk

K970977 is an FDA 510(k) clearance for the LATEX EXAMINATION GLOVES, POWDER FREE. Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Arista Medi Prima (Jakarta Barat, ID). The FDA issued a Cleared decision on June 27, 1997 after a review of 105 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.

View all Arista Medi Prima devices

FDA 510(k) Submission Details - K970977

510(k) Number K970977 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 14, 1997
Decision Date June 27, 1997
Days to Decision 105 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
24d faster than avg
Panel avg: 129d · This submission: 105d
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 439
Devices cleared under the same product code (LYY) and FDA review panel - the closest regulatory comparables to K970977.
ALLEGIANCE NON STERILE POWDER FREE LOW PROTEIN LATEX EXAMIATION GLOVES
K972291 · Allegiance Healthcare Corp. · Jul 1997
LATEX EXAMINATION GLOVES
K970770 · Oon Corp. Resources · Jul 1997
UNIJECT EXAMINATION GLOVES
K970191 · Uniject Gloves , Ltd. · Jul 1997
POWDER - FREE LATEX EXAMINATION GLOVES APPLICATION
K964826 · Kossan Latex Industries(M)Sdn Bhd · Jun 1997
LOW PROTEIN LATEX EXAMINATION GLOVES
K970222 · Kossan Latex Industries(M)Sdn Bhd · Jun 1997
POWDER-FREE LATEX EXAMINATION GLOVES
K964724 · Pwa Industries Sdn. Bhd. · Jun 1997