FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PREPOWDER VINYL PATIENT EXAMINATION GLOVES
K Number: K962026
·
Decision Sep 10, 1996
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
3
Review Days
110
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Basic Information
- Device Name
- PREPOWDER VINYL PATIENT EXAMINATION GLOVES
- K Number
- K962026
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Hong Huang Tang Industrial Co., Ltd.
- Date Received
- May 23, 1996
- Decision Date
- September 10, 1996
- 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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