Cleared Traditional

K111604 - LANO-E

K111604 is an FDA 510(k) clearance for LANO-E, manufactured by Ug Global Resources Sdn. Bhd.. The device is a Class 1 General Hospital device with product code LYY cleared through the Traditional 510(k) pathway after a 366-day FDA review.

K111604 · Ug Global Resources Sdn. Bhd. · General Hospital
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Optimized for regulatory review, auditing and printing
Jun 2012
Decision
366d
Days
Class 1
Risk

K111604 is an FDA 510(k) clearance for the LANO-E. Classified as Latex Patient Examination Glove (product code LYY), Class I - General Controls.

Submitted by Ug Global Resources Sdn. Bhd. (Costa Mesa, US). The FDA issued a Cleared decision on June 8, 2012 after a review of 366 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Ug Global Resources Sdn. Bhd. devices

FDA 510(k) Submission Details - K111604

510(k) Number K111604 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 08, 2011
Decision Date June 08, 2012
Days to Decision 366 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
237d slower than avg
Panel avg: 129d · This submission: 366d
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 268
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