FDA 510(k)
FDA class 1
Substantially Equivalent
🇮🇩 Indonesia
VINYL PATIENT EXAMINATION GLOVES
K Number: K964629
·
Decision Feb 10, 1997
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
3
Review Days
83
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Basic Information
- Device Name
- VINYL PATIENT EXAMINATION GLOVES
- K Number
- K964629
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Arista Medi Prima
- Date Received
- November 19, 1996
- Decision Date
- February 10, 1997
- 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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