Autozyme Immobilized Enzyme Coil

FDA 510(k) K771384 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK771384

Submission

Device name
Autozyme Immobilized Enzyme Coil
Applicant
Technicon Instruments Corp.
Mchenry, IL, US
Received
July 27, 1977
Decision date
August 22, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CFR – Hexokinase, Glucose
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1345
Specialty
Clinical Chemistry

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Questions and answers

When was Autozyme Immobilized Enzyme Coil cleared by the FDA?

Autozyme Immobilized Enzyme Coil (K771384) received a 510(k) decision of Substantially Equivalent on August 22, 1977, 26 days after the submission was received.

What is the product code of K771384?

The FDA product code is CFR – Hexokinase, Glucose, a Class II (moderate risk) device regulated under 21 CFR 862.1345.