FDA 510(k) FDA class 1 Substantially Equivalent 🇹🇼 Taiwan

BROTHERS VINYL, POWDERED, PATIENT EXAMINATION GLOVES

K Number: K990946 · Decision May 4, 1999
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
3
Review Days
43

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BROTHERS VINYL, POWDERED, PATIENT EXAMINATION GLOVES
K Number
K990946
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Long First (Xiamen) Co., Ltd.
Date Received
March 22, 1999
Decision Date
May 4, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYZ), ordered by most recent decision date.

View all

Other Clearances by Long First (Xiamen) Co., Ltd.

K Number Device Name
K031170 POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE BROTHERS
K991085 BROTHERS, VINYL, POWDER-FREE, PATIENT EXAMINATION GLOVES