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 | Device Class | Medical Specialty |
|---|---|---|---|
| LYY | Latex Patient Examination Glove | FDA class 1 | General Hospital |
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Other Clearances by SINTON LATEX CHEMICAL INDUSTRIES CO., LTD.
| K Number | Device Name | ||
|---|---|---|---|
| K891220 | SINTON LATEX EXAMINATION GLOVE | Mar 22, 1989 | Substantially Equivalent |