FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HICKMAN PLASTIC SUBCUTANEOUS PORT
K Number: K873213
·
Decision Oct 27, 1987
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
285
Applicant Total
566
Review Days
74
Basic Information
- Device Name
- HICKMAN PLASTIC SUBCUTANEOUS PORT
- K Number
- K873213
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5965
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- C.R. BARD, INC.
- Date Received
- August 14, 1987
- Decision Date
- October 27, 1987
- Product Code
- LJT
- 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 |
|---|---|---|---|
| LJT | Port & Catheter, Implanted, Subcutaneous, Intravascular | FDA class 2 | General Hospital |
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