FDA 510(k)
FDA class 1
Substantially Equivalent
🇲🇾 Malaysia
POWDER FREE LATEX EXAMINATION GLOVES
K Number: K935946
·
Decision Jun 21, 1994
Classifications
1
FEI Numbers
169
Registration Numbers
169
Same Product Code
1953
Applicant Total
4
Review Days
190
Basic Information
- Device Name
- POWDER FREE LATEX EXAMINATION GLOVES
- K Number
- K935946
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- CRANBERRY (M) SDN. BHD.
- Date Received
- December 13, 1993
- Decision Date
- June 21, 1994
- Product Code
- LYY
- 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 |
|---|---|---|---|
| LYY | Latex Patient Examination Glove | FDA class 1 | General Hospital |
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Other Clearances by CRANBERRY (M) SDN. BHD.
| K Number | Device Name | ||
|---|---|---|---|
| K984039 | CRANBERRY POWDER FREE LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESSS) | Mar 29, 1999 | Substantially Equivalent |
| K983334 | NITRILE POWDER FREE EXAMINATION GLOVES | Feb 19, 1999 | Substantially Equivalent |
| K890976 | PATIENT EXAMINATION GLOVE | Apr 18, 1989 | Substantially Equivalent |