FDA 510(k) FDA class 1 Substantially Equivalent 🇲🇾 Malaysia

POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES

K Number: K120963 · Decision Jun 29, 2012
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
4
Review Days
91

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Basic Information

Device Name
POWDER FREE NATURAL RUBBER LATEX EXAMINATION GLOVES
K Number
K120963
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medtexx Manufacturing Sdn. Bhd.
Date Received
March 30, 2012
Decision Date
June 29, 2012
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 Medtexx Manufacturing Sdn. Bhd.

K Number Device Name
K071740 CHLORINATED POWDER FREE NITRILE LATEX EXAMINATION GLOVES
K070821 POWDERED NATURAL RUBBER LATEX EXAMINATION GLOVES (PROTEIN LABEL CLAIM) 200 MICROGRAMS OR LESS OF TOTAL WATER EXTRACTABLE
K070072 NON-CHLORINATED POLYMER COATED POWDER-FREE NATURAL LATEX EXAMINATION GLOVES