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

SINTON LATEX EXAMINATION GLOVE

K Number: K892090 · Decision Apr 28, 1989
Classifications
1
FEI Numbers
169
Registration Numbers
169
Same Product Code
1953
Applicant Total
2
Review Days
25

Basic Information

Device Name
SINTON LATEX EXAMINATION GLOVE
K Number
K892090
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
SINTON LATEX CHEMICAL INDUSTRIES CO., LTD.
Date Received
April 3, 1989
Decision Date
April 28, 1989
Product Code
LYY
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
LYY Latex Patient Examination Glove

Similar 510(k) Clearances

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

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Other Clearances by SINTON LATEX CHEMICAL INDUSTRIES CO., LTD.

K Number Device Name
K891220 SINTON LATEX EXAMINATION GLOVE