510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K003872Substantially Equivalent

Guthrie Prime Powdered Latex Examination Gloves with Protein Content Labeling Claim (200 Micrograms or Less)

Guthrie Medicare Products (Melaka) Sdn Bhd, Great Neck NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003872 is the FDA 510(k) clearance record for GUTHRIE PRIME POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS), a class I device, cleared for Guthrie Medicare Products (Melaka) Sdn Bhd on under FDA product code LYY (Latex Patient Examination Glove). FDA's definition for product code LYY reads: "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...". FDA records list 12 510(k) clearances for Guthrie Medicare Products (Melaka) Sdn Bhd, from to . As of , FDA records show no recalls naming K003872.

Clearance record

Decision date
Received
(39 days to decision)
Product code
LYY Latex Patient Examination Glove
Regulation
21 CFR 880.6250
Device class
Class I
Review panel
General Hospital
Applicant
Guthrie Medicare Products (Melaka) Sdn Bhd 55 Northern Blvd., Suite 200, Great Neck NY
510(k) summary
Statement
Third party review
No

Clearances, product code LYY

Trailing 12 months

FDA records hold no clearances under product code LYY in the trailing twelve months.

FDA records show no clearances under product code LYY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LYY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260