SENSIBEAD EIA DIGOXIN KIT— 510(k) K840673
Substantially EquivalentTerumo Medical Corp.
FDA 510(k) clearance K840673 for SENSIBEAD EIA DIGOXIN KIT, Substantially Equivalent on 1984-03-12. Applicant: Terumo Medical Corp.. Device class: 2.
Clearance details
- Applicant
- Terumo Medical Corp.
- 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
- Elkton, MD, US
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More clearances from Terumo Medical Corp.
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