FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INFUMIX MIXING CONTAINER
K Number: K870052
·
Decision Feb 27, 1987
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
21
Review Days
51
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Basic Information
- Device Name
- INFUMIX MIXING CONTAINER
- K Number
- K870052
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5025
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Biodynamics Corp.
- Date Received
- January 7, 1987
- Decision Date
- February 27, 1987
- 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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|---|---|---|---|
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| K884033 | BIODYNAMICS MODEL 200 BODY COMPOSITION ANALYZER | Nov 17, 1988 | Substantially Equivalent |
| K881631 | BIODYNAMICS AUTOTRANSFUSION RESERVOIR | Sep 9, 1988 | Substantially Equivalent |
| K881968 | BIODYNAMICS MODEL BI-400 BODY COMPOSITION ANALYZER | Jul 28, 1988 | Substantially Equivalent |
| K874361 | BIODYNAMICS MODEL BI-300 BODY COMPOSITION ANALYZER | Mar 16, 1988 | Substantially Equivalent |
| K873807 | AUTOTRANSFUSION APPARATUS | Mar 9, 1988 | Substantially Equivalent |
| K874034 | ADR-22 AUTOMATIC DIALYZER REPROCESSOR | Oct 23, 1987 | Substantially Equivalent |
| K822716 | UNIVERSAL CENTRIFUGE | Sep 30, 1982 | Substantially Equivalent |
| K822715 | PLATELET CENTRIFUGE | Sep 30, 1982 | Substantially Equivalent |
| K822422 | BASIC CENTRIFUGE | Sep 2, 1982 | Substantially Equivalent |