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

SYNTHETIC POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

K Number: K992555 · Decision Oct 14, 1999
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
795
Applicant Total
10
Review Days
76

Basic Information

Device Name
SYNTHETIC POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
K Number
K992555
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SHIJIAZHUANG GREAT VISION PLASTIC PRODUCTS CO., LT
Date Received
July 30, 1999
Decision Date
October 14, 1999
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

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Other Clearances by SHIJIAZHUANG GREAT VISION PLASTIC PRODUCTS CO., LT

K Number Device Name
K102097 POWDER FREE VINYL PATIENT EXAMINATION GLOVES
K102093 POWDER FREE VINYL PATIENT EXAMINATION GLOVES
K031108 SYNTHETIC (WHITE) VINYL PATIENT EXAMINATION GLOVES-POWDER FREE
K021506 POWDERED (BLUE) NITRILE PATIENT EXAMINATION GLOVES
K014077 POWDER FREE (BLUE) NITRILE PATIENT EXAMINATION GLOVES
K002012 SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES
K002015 SYNTHETIC POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION GLOVES
K992554 SYNTHETIC POWDERED VINYL PATIENT EXAMINATION GLOVES
K992862 SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES