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

SHANGHAI GIANTMAX POWDERED CLEAR VINYL EXAMINATION GLOVES

K Number: K032745 · Decision Oct 17, 2003
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
2
Review Days
43

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Basic Information

Device Name
SHANGHAI GIANTMAX POWDERED CLEAR VINYL EXAMINATION GLOVES
K Number
K032745
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 Giantmax Plastic Product Corp.
Date Received
September 4, 2003
Decision Date
October 17, 2003
Product Code
LYZ
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
LYZ Vinyl Patient Examination Glove

Similar 510(k) Clearances

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

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Other Clearances by Shanghai Giantmax Plastic Product Corp.

K Number Device Name
K032746 SHANGHAI GIANTMAX CLEAR VINYL POWDER FREE EXAMINATION GLOVES