FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ATAC 4300 HEMATOLOGY CELL COUNTER
K Number: K863332
·
Decision Sep 29, 1986
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
129
Applicant Total
6
Review Days
33
Basic Information
- Device Name
- ATAC 4300 HEMATOLOGY CELL COUNTER
- K Number
- K863332
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5200
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- TURPEN LABORATORY SYSTEMS, INC.
- Date Received
- August 27, 1986
- Decision Date
- September 29, 1986
- 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 |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (GKL), ordered by most recent decision date.
Glocyte Automated Cell Counter System
FDA 510(k)
FDA Class 2
·Hematology
IQ 200 URINE ANALIZER BODY FLUIDS MODULE
FDA 510(k)
FDA Class 2
·Hematology
HEMOCUE WBC SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
MODIFICATION TO BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
IQ 200 URINE ANALYZER BODY FLUIDS MODULE
FDA 510(k)
FDA Class 2
·Hematology
SYSMEX POCH-100I
FDA 510(k)
FDA Class 2
·Hematology
Other Clearances by TURPEN LABORATORY SYSTEMS, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K870836 | ATAC 1500 CHEMISTRY ANALYZER | Apr 1, 1987 | Substantially Equivalent |
| K851321 | ATAC 2000 CHEMISTRY ANALYZER | Apr 25, 1985 | Substantially Equivalent |
| K843059 | ATAC 2000 | Oct 11, 1984 | Substantially Equivalent |
| K832115 | ATAC 3000 | Jan 10, 1984 | Substantially Equivalent |
| K832116 | ATAC 4700 HEMATOLOGY CELL COUNTER | Oct 20, 1983 | Substantially Equivalent |