FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GUTHRIE SHIELD BLUE LATEX EXAMINATION GLOVES, POWDERED WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)

K Number: K010054 · Decision Jan 26, 2001
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
12
Review Days
18

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Basic Information

Device Name
GUTHRIE SHIELD BLUE LATEX EXAMINATION GLOVES, POWDERED WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)
K Number
K010054
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Guthrie Medicare Products (Melaka) Sdn Bhd
Date Received
January 8, 2001
Decision Date
January 26, 2001
Product Code
LYY
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYY Latex Patient Examination Glove

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYY), ordered by most recent decision date.

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Other Clearances by Guthrie Medicare Products (Melaka) Sdn Bhd

K Number Device Name
K003922 NITRILE EXAMINATION GLOVES (POWERED)
K003985 POWDERFREE NITRILE PATIENT EXMINATION GLOVE
K010078 GUTHRIE SHIELD PLUS BLUE LATEX EXAMINATION GLOVES (POWDER-FREE)
K003872 GUTHRIE PRIME POWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (200 MICROGRAMS OR LESS)
K001049 GUTHRIE POWDER-FREE LATEX SURGICAL GLOVE WITH (50 MICROGRAMS OR LESS)
K001047 GUTHRIE LATEX SURGICAL GLOVE (PRE-POWDERED)
K000090 GUTHRIE PRIME POWDER-FREE CHLORINATED PATIENT EXAMINATION GLOVES
K993793 GUTHRIE PRIME PRE-POWDERED PATIENT LATEX EXAMINATION GLOVE
K990228 GUTHRIE PRIME POWDER-FREE
K954967 GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES
Search all 12 clearances from Guthrie Medicare Products (Melaka) Sdn Bhd →