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Stratus Cs Acute Care Betahcg and Nt-Probnp Testpak and Testpak Assay, Calpak and Dilpak

by Dade Behring, Inc.

510(k) K060548

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

2 closed

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK060548 Date6 Apr 2006ClearedStatusActive

Recalls

2 recalls · FDA

  • 2 recalls, same reason

    • Terminated Z-0617-2016 FDA Class II initiated 11 Nov 2015
    • Terminated Z-0615-2016 FDA Class II initiated 11 Nov 2015

    Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DHA
Device Class
Class II
Regulation
21 CFR Part 862.1155
Advisory Committee
Clinical Chemistry
FDA Decision
SESE Substantially Equivalent

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