Profile 750 Blood Cell Counter

FDA 510(k) K823886 · Mallinckrodt Critical Care

Substantially Equivalent

510(k) numberK823886

Submission

Device name
Profile 750 Blood Cell Counter
Applicant
Mallinckrodt Critical Care
Walker, MI, US
Received
December 27, 1982
Decision date
March 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 Profile 750 Blood Cell Counter cleared by the FDA?

Profile 750 Blood Cell Counter (K823886) received a 510(k) decision of Substantially Equivalent on March 1, 1983, 64 days after the submission was received.

What is the product code of K823886?

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