FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CRITHIDIA LUCILIAE NATIVE DNA-IFA TEST
K Number: K810301
·
Decision Feb 25, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
109
Applicant Total
36
Review Days
21
Basic Information
- Device Name
- CRITHIDIA LUCILIAE NATIVE DNA-IFA TEST
- K Number
- K810301
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5100
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- IMMUNO CONCEPTS, INC.
- Date Received
- February 4, 1981
- Decision Date
- February 25, 1981
- Product Code
- DHN
- 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 |
|---|---|---|---|
| DHN | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control | FDA class 2 | Immunology |
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