FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES
K Number: K950626
·
Decision May 5, 1995
Classifications
1
FEI Numbers
59
Registration Numbers
59
Same Product Code
376
Applicant Total
37
Review Days
84
Basic Information
- Device Name
- OPTICLONE CD3/CD4 MONOCLONAL ANTIBODIES
- K Number
- K950626
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.5220
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- IMMUNOTECH CORP.
- Date Received
- February 10, 1995
- Decision Date
- May 5, 1995
- Product Code
- GKZ
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| GKZ | Counter, Differential Cell | FDA class 2 | Hematology |
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