FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HUMAN IGG-ALBUMIN TEST KIT
K Number: K811178
·
Decision May 15, 1981
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
15
Review Days
17
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Basic Information
- Device Name
- HUMAN IGG-ALBUMIN TEST KIT
- K Number
- K811178
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1035
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Meloy Laboratories, Inc.
- Date Received
- April 28, 1981
- Decision Date
- May 15, 1981
- Product Code
- CJQ
- 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 |
|---|---|---|---|
| CJQ | Radial Immunodiffusion, Albumin | FDA class 2 | Clinical Chemistry |
Other Clearances by Meloy Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K852033 | SS-A(RO) & SS-B(LA) ANTIBODY ASSAY | Jun 21, 1985 | Substantially Equivalent |
| K844678 | MELOY LAB-ANTINUCLEAR ANTIBODY TEST-HEP-2 CELL CUL | Jan 4, 1985 | Substantially Equivalent |
| K841708 | MELOY IMMUNOSTAT MONOCLONAL FACTOR VIII | Jul 19, 1984 | Substantially Equivalent |
| K842247 | MELOY AUTOANTIBODY TEST SYS | Jun 26, 1984 | Substantially Equivalent |
| K831292 | ANTI-ENA TEST | Jul 18, 1983 | Substantially Equivalent |
| K820265 | ANA TEST (MOUSE LIVER SUBSTRATE) | Feb 12, 1982 | Substantially Equivalent |
| K820005 | TOTAL HEMOLYTIC COMPLEMENT TEST KIT | Jan 22, 1982 | Substantially Equivalent |
| K792562 | IMMUNOSTAT TSH TEST | Jan 16, 1980 | Substantially Equivalent |
| K791493 | ANTI-NUCLEAR ANTIBODY TEST | Sep 24, 1979 | Substantially Equivalent |
| K791065 | IMMUNOSPOT TSH TEST | Jul 30, 1979 | Substantially Equivalent |