FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IMMUNO DIAGNOSTICS ASSAY
K Number: K822026
·
Decision Aug 3, 1982
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
53
Applicant Total
280
Review Days
22
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Basic Information
- Device Name
- IMMUNO DIAGNOSTICS ASSAY
- K Number
- K822026
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5510
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Helena Laboratories
- Date Received
- July 12, 1982
- Decision Date
- August 3, 1982
- Product Code
- CZP
- Advisory Committee
- Immunology
- 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 |
|---|---|---|---|
| CZP | Iga, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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