Facs Analyzer

FDA 510(k) K832420 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK832420

Submission

Device name
Facs Analyzer
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Walker, MI, US
Received
July 22, 1983
Decision date
September 1, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKL – Counter, Cell, Automated (Particle Counter)
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5200
Specialty
Hematology

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Questions and answers

When was Facs Analyzer cleared by the FDA?

Facs Analyzer (K832420) received a 510(k) decision of Substantially Equivalent on September 1, 1983, 41 days after the submission was received.

What is the product code of K832420?

The FDA product code is GKL – Counter, Cell, Automated (Particle Counter), a Class II (moderate risk) device regulated under 21 CFR 864.5200.