FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE
K Number: K030200
·
Decision Mar 20, 2003
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
4
Review Days
58
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Basic Information
- Device Name
- POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE
- K Number
- K030200
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Kaohsiung Brothers Products Corp.
- Date Received
- January 21, 2003
- Decision Date
- March 20, 2003
- 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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