RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO— 510(k) K770365
Substantially EquivalentTravenol Laboratories, S.A.
FDA 510(k) clearance K770365 for RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO, Substantially Equivalent on 1977-02-24. Applicant: Travenol Laboratories, S.A..
Clearance details
- Applicant
- Travenol Laboratories, S.A.
- Product code
- Code DPO
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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