FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NDNA ANTIBODY TEST KIT
K Number: K874191
·
Decision Dec 18, 1987
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
28
Applicant Total
15
Review Days
65
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Basic Information
- Device Name
- NDNA ANTIBODY TEST KIT
- K Number
- K874191
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5100
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Lipogen, Inc.
- Date Received
- October 14, 1987
- Decision Date
- December 18, 1987
- Product Code
- LRM
- Advisory Committee
- Immunology
- 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 |
|---|---|---|---|
| LRM | Anti-Dna Antibody (Enzyme-Labeled), Antigen, Control | FDA class 2 | Immunology |
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Other Clearances by Lipogen, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K902636 | LIPOGEN RHEUMELISA DSDNA ASSAY | Jun 28, 1990 | Substantially Equivalent |
| K895997 | RHEUMELISA ASSAY FOR RNP AUTOANTIBODIES | Nov 6, 1989 | Substantially Equivalent |
| K895996 | RHEUMELISA ASSAY FOR SM AUTOANTIBODIES | Nov 6, 1989 | Substantially Equivalent |
| K895995 | RHEUMELISA ASSAY FOR SS-B/LA AUTOANTIBODIES | Oct 27, 1989 | Substantially Equivalent |
| K895994 | RHEUMELISA ASSAY FOR SS-A/RO AUTOANTIBODIES | Oct 24, 1989 | Substantially Equivalent |
| K894659 | ANA ANTISERA CONTROL KIT | Sep 21, 1989 | Substantially Equivalent |
| K892421 | MODIFIED ACCESS R-CLONE ANA/RF SCREENING TEST | May 9, 1989 | Substantially Equivalent |
| K885048 | ACCESS R-CLONE ANA PROFILE ASSAY | Jan 24, 1989 | Substantially Equivalent |
| K882740 | ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY | Sep 22, 1988 | Substantially Equivalent |
| K880254 | SM ANTIBODY TEST KIT | Apr 6, 1988 | Substantially Equivalent |