RADIOIMMUNOASSAY DIGOXIN TEST, IN VITRO— 510(k) K770365

Name: FDA 510(k) clearance K770365
Creator: U.S. Food and Drug Administration
Published: 1977-02-24

Substantially Equivalent

Travenol 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.. Device class: 2.

Clearance details

Applicant: Travenol Laboratories, S.A.
Product code: Code DPO
Device class: Class 2
Regulation: 21 CFR 862.3320
Advisory panel: Clinical Toxicology
Date received: 1977-02-23
Decision date: 1977-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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