FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SALICYLATE ASSAY KIT
K Number: K831336
·
Decision Jul 7, 1983
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
28
Applicant Total
38
Review Days
73
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Basic Information
- Device Name
- SALICYLATE ASSAY KIT
- K Number
- K831336
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.3830
- Medical Specialty
- Clinical Toxicology
- Decision
- Substantially Equivalent
- Applicant
- Quantimetrix Corp.
- Date Received
- April 25, 1983
- Decision Date
- July 7, 1983
- Product Code
- DKJ
- Advisory Committee
- Clinical Toxicology
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| DKJ | Colorimetry, Salicylate | FDA class 2 | Clinical Toxicology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (DKJ), ordered by most recent decision date.
ADVIA CHEMISTRY SALICYLATE REAGENT
FDA 510(k)
FDA Class 2
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SALICYLATE-SL ASSAY
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SALICYLATE ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEM
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FDA Class 2
·Clinical Toxicology
SYNCHRON SYSTEMS SALICYLATE REAGENT AND CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Toxicology
EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109UL
FDA 510(k)
FDA Class 2
·Clinical Toxicology
SALICYLATE-SL ASSAY CATALOGUE NUMBER 511-20,511-40
FDA 510(k)
FDA Class 2
·Clinical Toxicology
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