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Abuscreen Ontrak Pos. Ref. Control for Morphine

by Roche Diagnostic Systems, Inc. 510(k)

Active United States

510(k) K893856

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK893856 Date3 Aug 1989ClearedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
LAS
Device Class
Class I
Regulation
21 CFR Part 862.3280
Advisory Committee
Clinical Toxicology
FDA Decision
SESE Substantially Equivalent

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