FDA 510(k)
FDA class 1
Substantially Equivalent
🇨🇳 China
PVC EXAMINATION GLOVES
K Number: K894752
·
Decision Jan 11, 1990
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
795
Applicant Total
1
Review Days
169
Basic Information
- Device Name
- PVC EXAMINATION GLOVES
- K Number
- K894752
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- DAN DONG LINSEN PLASTIC INDUSTRIAL CO., LTD.
- Date Received
- July 26, 1989
- Decision Date
- January 11, 1990
- 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 | Device Class | Medical Specialty |
|---|---|---|---|
| LYZ | Vinyl Patient Examination Glove | FDA class 1 | General Hospital |
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