FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
QMS / MULTIGENT VALPROIC ACID REAGENT, PART #396075
K Number: K030405
·
Decision Apr 28, 2003
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
34
Applicant Total
2
Review Days
81
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Basic Information
- Device Name
- QMS / MULTIGENT VALPROIC ACID REAGENT, PART #396075
- K Number
- K030405
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3645
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Seradyn
- Date Received
- February 6, 2003
- Decision Date
- April 28, 2003
- Product Code
- LEG
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| LEG | Enzyme Immunoassay, Valproic Acid | FDA class 2 | Clinical Toxicology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (LEG), ordered by most recent decision date.
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Other Clearances by Seradyn
| K Number | Device Name | ||
|---|---|---|---|
| K023058 | QMS DIGOXIN REAGENT SYSTEM ON THE ABBOTT AEROSET SYSTEM | Oct 24, 2002 | Substantially Equivalent |