FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇳 China

GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES

K Number: K052923 · Decision Dec 21, 2005
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
2
Review Days
64

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Basic Information

Device Name
GREAT GLOVE POWDER FREE VINYL EXAMINATION GLOVES
K Number
K052923
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Great Glove (China), Inc.
Date Received
October 18, 2005
Decision Date
December 21, 2005
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 Great Glove (China), Inc.

K Number Device Name
K052922 GREAT GLOVE POWDERED VINYL EXAMINATION GLOVES