FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RUBELLA IGM
K Number: K921573
·
Decision Aug 27, 1992
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
14
Review Days
147
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Basic Information
- Device Name
- RUBELLA IGM
- K Number
- K921573
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3510
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Clark Laboratories, Inc.
- Date Received
- April 2, 1992
- Decision Date
- August 27, 1992
- Product Code
- LFX
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- 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 |
|---|---|---|---|
| LFX | Enzyme Linked Immunoabsorbent Assay, Rubella | FDA class 2 | Microbiology |
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Other Clearances by Clark Laboratories, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K980912 | VCA IGG ELISA TEST SYSTEM | Jul 22, 1998 | Substantially Equivalent |
| K980596 | VCA IGM ELISA TEST SYSTEM | Jul 22, 1998 | Substantially Equivalent |
| K980598 | EBNA-1 IGM ELISA TEST SYSTEM | May 1, 1998 | Substantially Equivalent |
| K973123 | EA-D IGG ELISA TEST SYSTEM | Mar 26, 1998 | Substantially Equivalent |
| K931543 | ENCORE ENA COMBINED EIA | Sep 8, 1993 | Substantially Equivalent |
| K925826 | ENCORE THYROGLOBULIN IGE, IGA AND IGM EIA | Jan 26, 1993 | Substantially Equivalent |
| K923537 | ENCORE DS-DNA | Dec 23, 1992 | Substantially Equivalent |
| K921870 | ENCORE SM/RNP | Dec 1, 1992 | Substantially Equivalent |
| K921572 | ENCORE SM | Dec 1, 1992 | Substantially Equivalent |
| K922340 | ENCORE SS-B | Oct 16, 1992 | Substantially Equivalent |