FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODIFIED INTRAVENOUS CATHETER
K Number: K896813
·
Decision Oct 19, 1990
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
1
Review Days
319
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Basic Information
- Device Name
- MODIFIED INTRAVENOUS CATHETER
- K Number
- K896813
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5200
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Safeguard Needle Co.
- Date Received
- December 4, 1989
- Decision Date
- October 19, 1990
- Product Code
- FOZ
- 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 |
|---|---|---|---|
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FDA class 2 | General Hospital |
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