Delta Test Amylase UV

FDA 510(k) K800049 · Bd Becton Dickinson Vacutainer Systems Preanalytic

Substantially Equivalent

510(k) numberK800049

Submission

Device name
Delta Test Amylase UV
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Washington, DC, US
Received
January 9, 1980
Decision date
January 23, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 Delta Test Amylase UV cleared by the FDA?

Delta Test Amylase UV (K800049) received a 510(k) decision of Substantially Equivalent on January 23, 1980, 14 days after the submission was received.

What is the product code of K800049?

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