Access Toxoplasma Igm Reagents on the Access Immunoassay Analyzer, Models 34460, 34465, 34469

FDA 510(k) K973448 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK973448

Submission

Device name
Access Toxoplasma Igm Reagents on the Access Immunoassay Analyzer, Models 34460, 34465, 34469
Applicant
Beckman Instruments, Inc.
Chaska, MN, US
Received
September 11, 1997
Decision date
September 17, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LGD – Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii
Device class
Class II (moderate risk)
Regulation
21 CFR 866.3780
Specialty
Microbiology

Other 510(k)s with product code LGD

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K242022Access Toxo IgGLGD · Traditional Beckman Coulter, Inc.03/28/2025SE
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K233932Alinity i Toxo IgMLGD · Traditional Abbott Laboratories08/30/2024SE
K210596ARCHITECT Toxo IgGLGD · Traditional Abbott Laboratories05/19/2022SE
K162678Elecsys Toxo IgM, Elecsys Toxo IgM PreciControlLGD · Traditional Roche Diagnostics06/23/2017SE
K142826ADVIA Centaur Toxoplasma M (Toxo M)LGD · Traditional Siemens Healthcare Diagnostics, Inc.12/22/2015SE
K132234Liaison(R) Toxo Igg II, Liaison(R) Control Toxo Igg IILGD · Traditional DiaSorin, Inc.08/28/2013SE
K131441Liaison Toxo Igm II, Liaison Control Toxo Igm IILGD · Traditional DiaSorin, Inc.08/09/2013SE
K101946Vidas Toxo Igg AvidityLGD · Traditional bioMerieux, Inc.05/18/2011SE
K102681Advia Centaur Toxoplasma Igg (Toxo G)LGD · Traditional Siemens Healthcare Diagnostics, Inc.05/04/2011SE

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Questions and answers

When was Access Toxoplasma Igm Reagents on the Access Immunoassay Analyzer, Models 34460, 34465, 34469 cleared by the FDA?

Access Toxoplasma Igm Reagents on the Access Immunoassay Analyzer, Models 34460, 34465, 34469 (K973448) received a 510(k) decision of Substantially Equivalent on September 17, 1998, 371 days after the submission was received.

What is the product code of K973448?

The FDA product code is LGD – Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii, a Class II (moderate risk) device regulated under 21 CFR 866.3780.