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

SYNTHETIC POWDERED (WHITE) VINYL PATIENT EXAMINATION GLOVES

K Number: K001863 · Decision Jul 11, 2000
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
4
Review Days
22

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Basic Information

Device Name
SYNTHETIC POWDERED (WHITE) VINYL PATIENT EXAMINATION GLOVES
K Number
K001863
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 Hongxiang Plastics Products Co; , Ltd.
Date Received
June 19, 2000
Decision Date
July 11, 2000
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 Shijiazhuang Hongxiang Plastics Products Co; , Ltd.

K Number Device Name
K001861 SYNTHETIC POWDERED (YELLOW) VINYL PATIENT EXAMINATION GLOVES
K001834 SYNTHETIC POWDER FREE (YELLOW) VINYL PATIENT EXAMINATION GLOVES
K001862 SYNTHETIC POWDER FREE (WHITE) VINYL PATIENT EXAMINATION GLOVES