FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
EUROIMMUN ENDOMYSIUM IFA: ESOPHAGUS (MONKEY) KIT
K Number: K061408
·
Decision Oct 5, 2006
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
39
Applicant Total
6
Review Days
136
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Basic Information
- Device Name
- EUROIMMUN ENDOMYSIUM IFA: ESOPHAGUS (MONKEY) KIT
- K Number
- K061408
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5660
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Euroimmun Us, LLC
- Date Received
- May 22, 2006
- Decision Date
- October 5, 2006
- Product Code
- MVM
- 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 |
|---|---|---|---|
| MVM | Autoantibodies, Endomysial(Tissue Transglutaminase) | FDA class 2 | Immunology |
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Other Clearances by Euroimmun Us, LLC
| K Number | Device Name | ||
|---|---|---|---|
| K070789 | EUROIMMUN ANTI-CCP ELISA | Dec 31, 2007 | Substantially Equivalent |
| K061239 | EUROIMMUN ANTI-HSV-2 ELISA (IGG) AND ANTI-HSV-1 ELISA (IGG) KIT | Jun 28, 2007 | Substantially Equivalent |
| K070763 | EUROIMMUN ANA IFA: HEP-20-10 | May 22, 2007 | Substantially Equivalent |
| K060700 | EUROIMMUN PR3 ELISA KIT. EUROIMMUN MPO ELISA KIT. | Sep 8, 2006 | Substantially Equivalent |
| K051489 | EUROIMMUN ANCA IFA GRANULOCYTE BIOCHIP MOSCAIC IGG ANTIBODY IN HUMAN SERUM | Feb 16, 2006 | Substantially Equivalent |