FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469
K Number: K032789
·
Decision Oct 9, 2003
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
844
Applicant Total
7
Review Days
31
Basic Information
- Device Name
- REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P1, MODEL BX10468, REPLACEMENT PUMP HEAD DOOR ASSEMBLY, P2, MODEL BX10469
- K Number
- K032789
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- AMERICAN I.V. PRODUCTS, INC.
- Date Received
- September 8, 2003
- Decision Date
- October 9, 2003
- Product Code
- FRN
- 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 |
|---|---|---|---|
| FRN | Pump, Infusion | FDA class 2 | General Hospital |
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