FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BLOOD CELL DILUENT 78N 1913
K Number: K822325
·
Decision Oct 18, 1982
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
37
Applicant Total
4
Review Days
76
Basic Information
- Device Name
- BLOOD CELL DILUENT 78N 1913
- K Number
- K822325
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.8200
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- INTERSCIENCE, INC.
- Date Received
- August 3, 1982
- Decision Date
- October 18, 1982
- Product Code
- GIF
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| GIF | Diluent, Blood Cell | FDA class 1 | Hematology |
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