DIGOXIN-EIA-XT— 510(k) K896863
Substantially EquivalentIn Vitro Diagnostics, Inc.
FDA 510(k) clearance K896863 for DIGOXIN-EIA-XT, Substantially Equivalent on 1990-02-13. Applicant: In Vitro Diagnostics, Inc.. Device class: 2.
Clearance details
- Applicant
- In Vitro Diagnostics, Inc.
- Product code
- Code KXT
- Device class
- Class 2
- Regulation
- 21 CFR 862.3320
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Littleton, CO, US
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More clearances from In Vitro Diagnostics, Inc.
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