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BD FACSCANTO II FLOW CYTOMETER - (5-3), Model 339473

by Bd Biosciences

510(k) K062087

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

3 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 · Special NumberK062087 Date14 Sep 2006ClearedStatusActive

Recalls

3 recalls · FDA

    • Terminated Z-2090-2015 FDA Class III initiated 15 Jun 2015

    Instruments installed between June 2007 and September 2011 do not contain labeling pursuant to the Food and Drug Administration's (FDA's) Guidance on Laser Products- Conformance with IEC 60825-1 and IEC 60601-2-22 (Laser Notice No. 50).

    • Terminated Z-1530-2008 FDA Unclassified (pre-2012) initiated 21 Dec 2007

    Values might not update in statistics views after certain functions are performed in a worksheet.

    • Terminated Z-1525-2008 FDA Unclassified (pre-2012) initiated 5 Apr 2007

    When data file containing one or no fluoresence parameters is exported, the software will automatically apply compensation to this file and all subsequently exported files.

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  • Withdrawn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
GKZ
Device Class
Class II
Regulation
21 CFR Part 864.5220
Advisory Committee
Hematology
FDA Decision
SESE Substantially Equivalent

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