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

SUNMAX VIETNAM CO. LTD POWDER FREE WHITE NITRILE EXAMINATION GLOVE

K Number: K101870 · Decision Dec 20, 2010
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
1
Review Days
167

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Basic Information

Device Name
SUNMAX VIETNAM CO. LTD POWDER FREE WHITE NITRILE EXAMINATION GLOVE
K Number
K101870
Device Class
FDA class 1
Clearance Type
Abbreviated
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sunmax Vietnam Co., Ltd.
Date Received
July 6, 2010
Decision Date
December 20, 2010
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

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