FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INFUSION PUMP
K Number: K831089
·
Decision Apr 28, 1983
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
5
Review Days
24
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Basic Information
- Device Name
- INFUSION PUMP
- K Number
- K831089
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.2910
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Beech Medical, Inc.
- Date Received
- April 4, 1983
- Decision Date
- April 28, 1983
- Product Code
- FLL
- 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 |
|---|---|---|---|
| FLL | Continuous Measurement Thermometer | FDA class 2 | General Hospital |
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