FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POWDERED VINYL EXAM GLOVES, WHITE
K Number: K031104
·
Decision Jun 10, 2003
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
798
Applicant Total
6
Review Days
64
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Basic Information
- Device Name
- POWDERED VINYL EXAM GLOVES, WHITE
- K Number
- K031104
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Glormed Intl., Inc.
- Date Received
- April 7, 2003
- Decision Date
- June 10, 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 |
Similar 510(k) Clearances
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Other Clearances by Glormed Intl., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K041945 | POWDER-FREE BLUE VINYL EXAM GLOVES | Aug 20, 2004 | Substantially Equivalent |
| K021353 | POWDER-FREE-VINYL EXAMINATION GLOVES, COLOR: WHITE | Jun 6, 2002 | Substantially Equivalent |
| K002340 | VINYL EXAMINATION GLOVE, POWDER-FREE, YELLOW | Aug 22, 2000 | Substantially Equivalent |
| K983494 | VINYL EXAM GLOVES, POWDER FREE | Nov 5, 1998 | Substantially Equivalent |
| K981360 | VINYL PATIENT EXAMINATION GLOVE, POWDERED | Oct 15, 1998 | Substantially Equivalent |