Amylase (Colorimetric) Reagent Set

FDA 510(k) K915710 · Tech Intl. Co.

Substantially Equivalent

510(k) numberK915710

Submission

Device name
Amylase (Colorimetric) Reagent Set
Applicant
Tech Intl. Co.
Rochester Hills, MI, US
Received
November 29, 1991
Decision date
January 30, 1992
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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More from Sentinel Ch. Srl

510(k)DeviceDecision
K915704Amylase (Kinetic) Reagent SetCJD · Traditional 06/28/1996SE
K915705Acid Phosphatase Reagent SetCKE · Traditional 02/27/1992SE
K915707Ammonia Reagent SetJIF · Traditional 02/26/1992SE
K914158Uric Acid Reagent SetKNK · Traditional 02/21/1992SE
K915706Lipase Reagent SetCET · Traditional 02/18/1992SE
K914160Cholesterol Regeant SetCHH · Traditional 01/30/1992SE
K915709Creatine Kinase-Mb (Ck-Mb) Reagent SetCGS · Traditional 01/27/1992SE
K914159Glucose Reagent SetCGA · Traditional 01/27/1992SE
K915708Inorganic Phosphorus(Colorimetric) Reagent SetCEO · Traditional 01/22/1992SE
K914171In Vitro Diagnostic Regeant Set,CholinesteraseDIH · Traditional 12/18/1991SE

Questions and answers

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

Amylase (Colorimetric) Reagent Set (K915710) received a 510(k) decision of Substantially Equivalent on January 30, 1992, 62 days after the submission was received.

What is the product code of K915710?

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