Atellica CH Amylase_2 (AMY_2)

FDA 510(k) K191454 · Siemens Healthcare Diagnostics, Inc.

Substantially Equivalent

510(k) numberK191454

Submission

Device name
Atellica CH Amylase_2 (AMY_2)
Applicant
Siemens Healthcare Diagnostics, Inc.
Newark, DE, US
Received
May 31, 2019
Decision date
July 30, 2019
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

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K130685Hitachi Clinical Analyzer S Test Reagent Cartridges for LD and AmyJFJ · Traditional Hitachi Chemical Diagnostics, Inc.08/09/2013SE
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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
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Questions and answers

When was Atellica CH Amylase_2 (AMY_2) cleared by the FDA?

Atellica CH Amylase_2 (AMY_2) (K191454) received a 510(k) decision of Substantially Equivalent on July 30, 2019, 60 days after the submission was received.

What is the product code of K191454?

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