FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ATAC 3000
K Number: K832115
·
Decision Jan 10, 1984
Classifications
1
FEI Numbers
174
Registration Numbers
174
Same Product Code
207
Applicant Total
6
Review Days
194
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Basic Information
- Device Name
- ATAC 3000
- K Number
- K832115
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2160
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Turpen Laboratory Systems, Inc.
- Date Received
- June 30, 1983
- Decision Date
- January 10, 1984
- Product Code
- JJE
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JJE | Analyzer, Chemistry (Photometric, Discrete), For Clinical Use | FDA class 1 | Clinical Chemistry |
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Other Clearances by Turpen Laboratory Systems, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K870836 | ATAC 1500 CHEMISTRY ANALYZER | Apr 1, 1987 | Substantially Equivalent |
| K863332 | ATAC 4300 HEMATOLOGY CELL COUNTER | Sep 29, 1986 | Substantially Equivalent |
| K851321 | ATAC 2000 CHEMISTRY ANALYZER | Apr 25, 1985 | Substantially Equivalent |
| K843059 | ATAC 2000 | Oct 11, 1984 | Substantially Equivalent |
| K832116 | ATAC 4700 HEMATOLOGY CELL COUNTER | Oct 20, 1983 | Substantially Equivalent |