Cedia Digoxin

by Boehringer Mannheim Corp. 510(k)

Active United States

510(k) K970881

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK970881	Date14 May 1997Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 12 Oct 2026.

Specification

510(k)

510(k) Number: K970881
FDA Product Code: KXT

Device Class: Class II
Regulation: 21 CFR Part 862.3320
Advisory Committee: Clinical Toxicology
FDA Decision: SESE Substantially Equivalent

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