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

SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVES

K Number: K021001 · Decision May 16, 2002
Classifications
1
FEI Numbers
380
Registration Numbers
380
Same Product Code
1171
Applicant Total
4
Review Days
49

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Basic Information

Device Name
SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVES
K Number
K021001
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Shanghai Glovmax Enterprise Co.,Ltd
Date Received
March 28, 2002
Decision Date
May 16, 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

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

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Other Clearances by Shanghai Glovmax Enterprise Co.,Ltd

K Number Device Name
K021000 SHANGHAI GLOVMAX ENTERPRISE POWDERED BLUE NITRILE EXAMINATION GLOVES
K993880 SHANGHAI GLOVMAX ENTERPRISE CO, LTD., POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K993859 SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION GLOVES