FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
GENESIS I AUTOMATED CELL COUNTER
K Number: K910679
·
Decision May 7, 1991
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
2
Review Days
81
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Basic Information
- Device Name
- GENESIS I AUTOMATED CELL COUNTER
- K Number
- K910679
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5200
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Alicia Diagnostics, Inc.
- Date Received
- February 15, 1991
- Decision Date
- May 7, 1991
- Product Code
- GKL
- 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 |
|---|---|---|---|
| GKL | Counter, Cell, Automated (Particle Counter) | FDA class 2 | Hematology |
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Other Clearances by Alicia Diagnostics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K925909 | GENESIS 1, AUTOMATED CELL COUNTER, MODIFICATION | Oct 27, 1994 | Substantially Equivalent |