RANDOX DIGITOXIN— 510(k) K012112

Substantially Equivalent

Randox Laboratories, Ltd.

FDA 510(k) clearance K012112 for RANDOX DIGITOXIN, Substantially Equivalent on 2002-01-11. Applicant: Randox Laboratories, Ltd..

Clearance details

Applicant: Randox Laboratories, Ltd.
Product code: Code LFM
Advisory panel: Clinical Toxicology
Date received: 2001-07-06
Decision date: 2002-01-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crumlin, GB

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