Technicon H*1 System Sub-Classification Luc Cat.

FDA 510(k) K852988 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK852988

Submission

Device name
Technicon H*1 System Sub-Classification Luc Cat.
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
July 15, 1985
Decision date
January 21, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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Questions and answers

When was Technicon H*1 System Sub-Classification Luc Cat. cleared by the FDA?

Technicon H*1 System Sub-Classification Luc Cat. (K852988) received a 510(k) decision of Substantially Equivalent on January 21, 1986, 190 days after the submission was received.

What is the product code of K852988?

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