Cleared Traditional

K790540 - RIA TEST KIT, CENTRIA DIGOXIN
(FDA 510(k) Clearance)

Apr 1979
Decision
34d
Days
Class 2
Risk

K790540 is an FDA 510(k) clearance for the RIA TEST KIT, CENTRIA DIGOXIN. This device is classified as a Radioimmunoassay, Digoxin (125-i), Rabbit Antibody, Charcoal Sep. (Class II - Special Controls, product code DPB).

Submitted by Ventrex Laboratories, Inc. (Walker, US). The FDA issued a Cleared decision on April 23, 1979, 34 days after receiving the submission on March 20, 1979.

This device falls under the Toxicology FDA review panel. Regulated under 21 CFR 862.3320.

Submission Details

510(k) Number K790540 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 20, 1979
Decision Date April 23, 1979
Days to Decision 34 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary

Device Classification

Product Code DPB — Radioimmunoassay, Digoxin (125-i), Rabbit Antibody, Charcoal Sep.
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.3320

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