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

GLOVE, PATIENT EXAMINATION, VINYL (POWDERED)

K Number: K964321 · Decision Jan 9, 1997
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
6
Review Days
72

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Basic Information

Device Name
GLOVE, PATIENT EXAMINATION, VINYL (POWDERED)
K Number
K964321
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 Hongray Plastic Products Co., Ltd.
Date Received
October 29, 1996
Decision Date
January 9, 1997
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 Hongray Plastic Products Co., Ltd.

K Number Device Name
K994206 SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES, BEIGE COLOR
K994222 SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, BEIGE COLOR
K992922 SENSI-PRO, DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR
K992860 DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES, WHITE COLOR
K982720 H-RAY