FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MDA PROTEIN ASSAY
K Number: K925617
·
Decision Jan 27, 1994
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
189
Applicant Total
130
Review Days
447
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Basic Information
- Device Name
- MDA PROTEIN ASSAY
- K Number
- K925617
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 864.7290
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Organon Teknika Corp.
- Date Received
- November 6, 1992
- Decision Date
- January 27, 1994
- Product Code
- GGP
- 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 |
|---|---|---|---|
| GGP | Test, Qualitative And Quantitative Factor Deficiency | FDA class 2 | Hematology |
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| K992401 | BACT/ALERT PF | Sep 3, 1999 | Substantially Equivalent |