FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CONTRAST CONTROL DEVICE
K Number: K982123
·
Decision Jul 21, 1998
Classifications
1
FEI Numbers
437
Registration Numbers
437
Same Product Code
1167
Applicant Total
48
Review Days
35
Basic Information
- Device Name
- CONTRAST CONTROL DEVICE
- K Number
- K982123
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- MEDEX, INC.
- Date Received
- June 16, 1998
- Decision Date
- July 21, 1998
- Product Code
- FPA
- 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | FDA class 2 | General Hospital |
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