FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CELL-DYN 1400 MULTI-PARAMETER AUTOMATED HEMATOLOGY
K Number: K903665
·
Decision Oct 4, 1990
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
73
Review Days
50
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Basic Information
- Device Name
- CELL-DYN 1400 MULTI-PARAMETER AUTOMATED HEMATOLOGY
- K Number
- K903665
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5220
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Unipath , Ltd.
- Date Received
- August 15, 1990
- Decision Date
- October 4, 1990
- Product Code
- GKZ
- 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 |
|---|---|---|---|
| GKZ | Counter, Differential Cell | FDA class 2 | Hematology |
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