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

POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR

K Number: K011791 · Decision Aug 1, 2001
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
7
Review Days
54

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Basic Information

Device Name
POWDER FREE NITRILE EXAMINATION GLOVES, VIOLET COLOR
K Number
K011791
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Latexx Partners Bhd.
Date Received
June 8, 2001
Decision Date
August 1, 2001
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

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

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Other Clearances by Latexx Partners Bhd.

K Number Device Name
K011792 NON-CHLORINATED, POLYMER COATED POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES
K992924 QTEXX, NON-CHLORINATED, POWDER FREE NITRILE EXAMINATION GLOVES, POLYMER-COATED
K992671 QTEXX PRE-POWDERED NITRILE EXAMINATION GLOVES
K991462 QTEXX POWDER FREE LATEX EXAMINATION GLOVES, POLYMER COATED
K981767 QTEXX POWDERFREE LATEX EXAMINATION GLOVES
K981159 PROFLEX POWDER FREE NITRILE EXAMINATION GLOVES