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

CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA

K Number: K013774 · Decision Mar 5, 2002
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
9
Review Days
112

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Basic Information

Device Name
CHLORINATED POWDER FREE NITRILE MEDICAL EXAMINATION GLOVES WITH ALOE VERA
K Number
K013774
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Supermax Sdn Bhd
Date Received
November 13, 2001
Decision Date
March 5, 2002
Product Code
LZA
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
LZA Polymer Patient Examination Glove

Similar 510(k) Clearances

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Other Clearances by Supermax Sdn Bhd

K Number Device Name
K993865 GREEN PEPPERMINT FLAVORED POWDERED LATEX EXAMINATION GLOVES
K993864 COLORED AND FLAVORED POWDER FREE LATEX EXAMINATION GLOVES
K993258 SUPERGLOVES, POWDER FREE NITRILE EXAMINATION GLOVES
K991415 SUPERGLOVES, POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES
K980966 SUPERGLOVES POWDERED NITRILE
K980494 SUPERGLOVES
K915251 PATIENT EXAMINATION LATEX GLOVES, HYPOALLERGENIC
K892287 PATIENT EXAMINATION GLOVES (LATEX)