IL TEST URIC ACID— 510(k) K931350
Substantially EquivalentInstrumentation Laboratory CO
FDA 510(k) clearance K931350 for IL TEST URIC ACID, Substantially Equivalent on 1993-10-01. Applicant: Instrumentation Laboratory CO. Device class: 1.
Clearance details
- Applicant
- Instrumentation Laboratory CO
- Product code
- Code KNK
- Device class
- Class 1
- Regulation
- 21 CFR 862.1775
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lexington, MA, US
Recent devices under product code KNK
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