Amylase2

FDA 510(k) K210633 · Abbott Ireland Diagnostics Division

Substantially Equivalent

510(k) numberK210633

Submission

Device name
Amylase2
Applicant
Abbott Ireland Diagnostics Division
Longsford, IE
Received
March 3, 2021
Decision date
May 26, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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

Other 510(k)s with product code JFJ

510(k)DeviceApplicantDecision
K191454Atellica CH Amylase_2 (AMY_2)JFJ · Traditional Siemens Healthcare Diagnostics, Inc.07/30/2019SE
K182474alpha-AMYLASE DIRECT, alpha-AMYLASE EPS, alpha-AMYLASE PANCREATIC, BILIRUBIN DIRECT…JFJ · Traditional Biosystems S.A.05/02/2019SE
K130685Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and AmyJFJ · Traditional Hitachi Chemical Diagnostics, Inc.08/09/2013SE
K122858Eltech Chinical System Amylase SL Elitech Clinical Systems ELICAL2 Eltech Clinical…JFJ · Traditional Elitechgroup10/03/2012SE
K091846Synchron Systems G7 Amylase (AMY7) Reagent with Model(S) A71607JFJ · Traditional Beckman Coulter, Inc.10/16/2009SE
K080823Easyra Amylase, Bun, Glu-H, Trig, Uric ReagentJFJ · Traditional Medica Corp.11/17/2008SE
K070064Amylase Eps ReagentJFJ · Traditional Thermo Fisher Scientific05/22/2007SE
K062180Abx Pentra Amylase CP; Multical; N Control; P Control; Clean-Chem CP; Clean-Chem 99 CPJFJ · Traditional Horiba Abx10/02/2006SE
K051447Sentinel Pancreatic AmylaseJFJ · Traditional Sentinel Ch. Srl01/26/2006SE
K040920Amylase Liquid Reagent, Model A532-200JFJ · Special Teco Diagnostics05/10/2004SE

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Questions and answers

When was Amylase2 cleared by the FDA?

Amylase2 (K210633) received a 510(k) decision of Substantially Equivalent on May 26, 2022, 449 days after the submission was received.

What is the product code of K210633?

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