T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT— 510(k) K896925
Substantially EquivalentIn Vitro Diagnostics, Inc.
FDA 510(k) clearance K896925 for T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT, Substantially Equivalent on 1990-01-18. Applicant: In Vitro Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- In Vitro Diagnostics, Inc.
- Product code
- Code KHQ
- Device class
- Class 2
- Regulation
- 21 CFR 862.1715
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Littleton, CO, US
Recent devices under product code KHQ
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