Amylase Reagent Set (Kinetic)

FDA 510(k) K931080 · Teco Diagnostics

Substantially Equivalent

510(k) numberK931080

Submission

Device name
Amylase Reagent Set (Kinetic)
Applicant
Teco Diagnostics
Placentia, CA, US
Received
March 2, 1993
Decision date
November 5, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JFJ – Catalytic Methods, Amylase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1070
Specialty
Clinical Chemistry

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Questions and answers

When was Amylase Reagent Set (Kinetic) cleared by the FDA?

Amylase Reagent Set (Kinetic) (K931080) received a 510(k) decision of Substantially Equivalent on November 5, 1993, 248 days after the submission was received.

What is the product code of K931080?

The FDA product code is JFJ – Catalytic Methods, Amylase, a Class II (moderate risk) device regulated under 21 CFR 862.1070.