FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LIQUID IMMUNOLOGY CONTROL LEVEL I, II, III
K Number: K963085
·
Decision Aug 20, 1996
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
7
Review Days
12
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Basic Information
- Device Name
- LIQUID IMMUNOLOGY CONTROL LEVEL I, II, III
- K Number
- K963085
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- International Enzymes, Inc.
- Date Received
- August 8, 1996
- Decision Date
- August 20, 1996
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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Other Clearances by International Enzymes, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K011169 | HSCRP CONTROL LEVEL 1, HSCRP CONTROL LEVEL 2, AND HSCRP CONTROL LEVEL 3 | May 18, 2001 | Substantially Equivalent |
| K953927 | LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM | Sep 15, 1995 | Substantially Equivalent |
| K953926 | LINICAL PROTEIN III CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN ARRAY PROTEIN SYSTEM | Sep 15, 1995 | Substantially Equivalent |
| K950802 | LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - FOR BECKMAN ARRAY 360 SYSTEM | Jun 1, 1995 | Substantially Equivalent |
| K944486 | LINICAL PROTEIN I CALIBRATION VERIFIERS LEVELS A - E | Dec 2, 1994 | Substantially Equivalent |
| K944513 | LINICAL PROTEIN VI CALIBRATION VERIFIERS LEVELS A-E | Dec 2, 1994 | Substantially Equivalent |