FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
QUALITROL CARDIAC MARKER CONTROL, LEVELS, 1,2 AND 3
K Number: K993715
·
Decision Nov 16, 1999
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
5
Review Days
13
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Basic Information
- Device Name
- QUALITROL CARDIAC MARKER CONTROL, LEVELS, 1,2 AND 3
- K Number
- K993715
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Seracare Technology
- Date Received
- November 3, 1999
- Decision Date
- November 16, 1999
- Product Code
- JJT
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- IM
- 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 |
|---|---|---|---|
| JJT | Enzyme Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
Similar 510(k) Clearances
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LIQUICHEK CARDIAC MARKERS CONTROL LT LEVEL 1,2,3, MODELS 646,647,648
FDA 510(k)
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·Clinical Chemistry
Other Clearances by Seracare Technology
| K Number | Device Name | ||
|---|---|---|---|
| K992939 | QUALITROL IMMUNOASSAY PLUS CONTROL, LEVELS 1,2 AND 3 | Dec 9, 1999 | Substantially Equivalent |
| K993631 | QUALITROL TUMOR MARKER CONTROL, LEVELS 1 AND 2 | Dec 9, 1999 | Substantially Equivalent |
| K992770 | QUALITROL IMMUNOLOGY CONTROL, LEVEL 1, 2 AND 3 | Nov 12, 1999 | Substantially Equivalent |
| K992395 | URINE DRUG SCREENING CONTROL | Aug 26, 1999 | Substantially Equivalent |