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

BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES

K Number: K022091 · Decision Dec 30, 2002
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
3
Review Days
186

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Basic Information

Device Name
BALDUR BRAND VINYL POWDER-FREE EXAMINATION GLOVES
K Number
K022091
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tangshan Zhonghong Pulin Group Co., Ltd.
Date Received
June 27, 2002
Decision Date
December 30, 2002
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 Tangshan Zhonghong Pulin Group Co., Ltd.

K Number Device Name
K082598 POWDER FREE BLUE PATIENT NITRILE EXAMINATION GLOVE
K022336 BALDUR BRAND VINYL POWDERED EXAMINATION GLOVES, SUN FLOWER GLOVES CO., LTD