FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INTRAVASCULAR ADMINISTRATION SET
K Number: K891919
·
Decision May 5, 1989
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
7
Review Days
39
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Basic Information
- Device Name
- INTRAVASCULAR ADMINISTRATION SET
- K Number
- K891919
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5570
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Multi-Med, Inc.
- Date Received
- March 27, 1989
- Decision Date
- May 5, 1989
- Product Code
- FMI
- 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 |
|---|---|---|---|
| FMI | Needle, Hypodermic, Single Lumen | FDA class 2 | General Hospital |
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Other Clearances by Multi-Med, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K890424 | ENTERAL FEEDING CONTAINER | Jun 14, 1989 | Substantially Equivalent |
| K890396 | EXTERNAL FEEDING SET FOR PUMP USE | May 23, 1989 | Substantially Equivalent |
| K891176 | INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION) | May 18, 1989 | Substantially Equivalent |
| K891072 | INTRAVASCULAR ADMINISTRATION SET | Apr 21, 1989 | Substantially Equivalent |
| K890340 | INTRAVASCULAR ADMINISTRATION SET | Mar 31, 1989 | Substantially Equivalent |
| K890127 | INTRAVASCULAR ADMINISTRATION SET | Feb 3, 1989 | Substantially Equivalent |