Cleared Traditional

K000611 - STELLER CD61 ASSAY FOR USE ON THE IMAGN 2000 MICROVOLUME FLUORIMETER
(FDA 510(k) Clearance)

May 2000
Decision
85d
Days
Class 2
Risk

K000611 is an FDA 510(k) clearance for the STELLER CD61 ASSAY FOR USE ON THE IMAGN 2000 MICROVOLUME FLUORIMETER. This device is classified as a Counter, Differential Cell (Class II - Special Controls, product code GKZ).

Submitted by Bd Biosciences (San Jose, US). The FDA issued a Cleared decision on May 18, 2000, 85 days after receiving the submission on February 23, 2000.

This device falls under the Hematology FDA review panel. Regulated under 21 CFR 864.5220.

Submission Details

510(k) Number K000611 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 23, 2000
Decision Date May 18, 2000
Days to Decision 85 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary Summary PDF

Device Classification

Product Code GKZ — Counter, Differential Cell
Device Class Class II - Special Controls
CFR Regulation 21 CFR 864.5220