FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DIASORIN LIAISON CMV IGM/IGG
K Number: K040290
·
Decision Jun 1, 2005
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
57
Applicant Total
2
Review Days
481
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Basic Information
- Device Name
- DIASORIN LIAISON CMV IGM/IGG
- K Number
- K040290
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.3175
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Diasorin S.P.A
- Date Received
- February 6, 2004
- Decision Date
- June 1, 2005
- Product Code
- LFZ
- 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 |
|---|---|---|---|
| LFZ | Enzyme Linked Immunoabsorbent Assay, Cytomegalovirus | FDA class 2 | Microbiology |
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Other Clearances by Diasorin S.P.A
| K Number | Device Name | ||
|---|---|---|---|
| K052499 | DIASORIN LIAISON TOXO IGG AND LIAISON TOXO IGM ASSAYS | Feb 8, 2006 | Substantially Equivalent |