FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DECANTER MODELS-VARIOUS
K Number: K830232
·
Decision Feb 9, 1983
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
1
Review Days
15
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Basic Information
- Device Name
- DECANTER MODELS-VARIOUS
- K Number
- K830232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5025
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Steri-Sytems, Corp.
- Date Received
- January 25, 1983
- Decision Date
- February 9, 1983
- Product Code
- KPE
- 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 |
|---|---|---|---|
| KPE | Container, I.V. | FDA class 2 | General Hospital |
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