FDA 510(k)
FDA class 1
Unknown
🇺🇸 United States
FAMILY FIRST AID KIT
K Number: K935131
·
Decision Mar 23, 1994
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
3
Review Days
146
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Basic Information
- Device Name
- FAMILY FIRST AID KIT
- K Number
- K935131
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6250
- Medical Specialty
- General Hospital
- Decision
- Unknown
- Statement or Summary
- Statement
- Applicant
- Medical Technologies International, Inc.
- Date Received
- October 28, 1993
- Decision Date
- March 23, 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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