BD Facs Sample Prep Assistant III (SPA III)

FDA 510(k) K102064 · Becton, Dickinson & CO

Substantially Equivalent

510(k) numberK102064

Submission

Device name
BD Facs Sample Prep Assistant III (SPA III)
Applicant
Becton, Dickinson & CO
San Jose, CA, US
Received
July 23, 2010
Decision date
March 7, 2011
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GKZ – Counter, Differential Cell
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5220
Specialty
Hematology

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K243283Alinity h-series SystemGKZ · Traditional Abbott Laboratories02/20/2025SE
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K240252UniCel DxH 900 Coulter Cellular Analysis System; UniCel DxH Slidemaker Stainer II…GKZ · Traditional Beckman Coulter, Inc.07/05/2024SE
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K240636HemoScreen Hematology AnalyzerGKZ · Abbreviated Pixcell Medical Technologies05/02/2024SE

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Questions and answers

When was BD Facs Sample Prep Assistant III (SPA III) cleared by the FDA?

BD Facs Sample Prep Assistant III (SPA III) (K102064) received a 510(k) decision of Substantially Equivalent on March 7, 2011, 227 days after the submission was received.

What is the product code of K102064?

The FDA product code is GKZ – Counter, Differential Cell, a Class II (moderate risk) device regulated under 21 CFR 864.5220.