FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
CYCLOSPORIN A (WHOLE BLOOD) CONTROL - LEVELS 1,2,3
K Number: K864456
·
Decision May 6, 1987
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
82
Applicant Total
12
Review Days
174
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Basic Information
- Device Name
- CYCLOSPORIN A (WHOLE BLOOD) CONTROL - LEVELS 1,2,3
- K Number
- K864456
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.3280
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Cala Diagnostics
- Date Received
- November 13, 1986
- Decision Date
- May 6, 1987
- Product Code
- LAS
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| LAS | Drug Specific Control Materials | FDA class 1 | Clinical Toxicology |
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Other Clearances by Cala Diagnostics
| K Number | Device Name | ||
|---|---|---|---|
| K944247 | CARDIOCHEX CKMB IMMUNOINHIBITION CONTROL | Oct 31, 1994 | Substantially Equivalent |
| K944246 | CARDIOCHEX CKMB MASS MEASUREMENT CONTROL | Oct 31, 1994 | Substantially Equivalent |
| K944243 | CARDIOCHEX | Oct 27, 1994 | Substantially Equivalent |
| K930874 | LD-1 CONTROL-LEVEL 1 & 2 | Apr 22, 1993 | Substantially Equivalent |
| K930875 | CKMB CONTROL - LEVEL 1,2,3 | Apr 13, 1993 | Substantially Equivalent |
| K930873 | CKMB ISOENZYME CONTROL-LEVEL 1,2.3 | Apr 13, 1993 | Substantially Equivalent |
| K926015 | CKMB CONTROL FOR MASS MEASUREMENT-LEVELS 1,2,3 | Dec 28, 1992 | Substantially Equivalent |
| K915503 | FIBRINOGEN FDP CONTROL | Jan 30, 1992 | Substantially Equivalent |
| K912827 | SERUM ALCOHOL CONTROL LEVELS 1, 2 & 3 | Aug 12, 1991 | Substantially Equivalent |
| K912826 | WHOLE BLOOD ALCOHOL CONTROL, LEVEL 1 & 2 | Jul 26, 1991 | Substantially Equivalent |