FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
FIBRIN(OGEN) FDP CONTROL LEVEL 1 & LEVEL 2
K Number: K932657
·
Decision Nov 2, 1993
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
56
Applicant Total
16
Review Days
153
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Basic Information
- Device Name
- FIBRIN(OGEN) FDP CONTROL LEVEL 1 & LEVEL 2
- K Number
- K932657
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7320
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- More Diagnostics
- Date Received
- June 2, 1993
- Decision Date
- November 2, 1993
- Product Code
- DAP
- 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 |
|---|---|---|---|
| DAP | Fibrinogen And Fibrin Split Products, Antigen, Antiserum, Control | FDA class 2 | Hematology |
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