DIGOXIN-EIA-XT
FDA 510(k) clearance K896863 · decided 1990-02-13
Clearance details
- K-number
- K896863
- Device name
- DIGOXIN-EIA-XT
- Applicant
- In Vitro Diagnostics, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1989-12-06
- Decision date
- 1990-02-13
- Days to decision
- 69 days
- Clearance type
- Traditional
- Product code
- KXT
- Device class
- 2
- Regulation number
- 862.3320
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- Location
- Littleton, CO, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch In Vitro Diagnostics
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.