FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SERUM COMPLEMENT ACTIVITY TEST-SCAT
K Number: K841541
·
Decision Jun 1, 1984
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
27
Applicant Total
2
Review Days
46
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Basic Information
- Device Name
- SERUM COMPLEMENT ACTIVITY TEST-SCAT
- K Number
- K841541
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.5240
- Medical Specialty
- Immunology
- Decision
- Substantially Equivalent
- Applicant
- Collaborative Research, Inc.
- Date Received
- April 16, 1984
- Decision Date
- June 1, 1984
- Product Code
- DAK
- 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 |
|---|---|---|---|
| DAK | Complement C1q, Antigen, Antiserum, Control | FDA class 2 | Immunology |
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Other Clearances by Collaborative Research, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K840241 | THYROXINE EMIA | Mar 30, 1984 | Substantially Equivalent |