Atlas FDA

TOXOPLASMA GONDII (TOXO) IGM ENZYME-LINKED IMMUNO

FDA 510(k) clearance K920702 · decided 1992-07-08

Clearance details

K-number
K920702
Device name
TOXOPLASMA GONDII (TOXO) IGM ENZYME-LINKED IMMUNO
Applicant
Pharmacia Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1992-02-18
Decision date
1992-07-08
Days to decision
141 days
Clearance type
Traditional
Product code
LGD
Device class
2
Regulation number
866.3780
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Fairfield, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
Access Toxo IgG (K242022)Beckman Coulter, Inc.2025-03-28
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Alinity i Toxo IgM (K233932)Abbott Laboratories2024-08-30
ARCHITECT Toxo IgG (K210596)Abbott Laboratories2022-05-19
Elecsys Toxo IgM, Elecsys Toxo IgM PreciControl (K162678)Roche Diagnostics2017-06-23
ADVIA Centaur Toxoplasma M (Toxo M) (K142826)Siemens Healthcare Diagnostics, Inc.2015-12-22
LIAISON(R) TOXO IGG II, LIAISON(R) CONTROL TOXO IGG II (K132234)DiaSorin, Inc.2013-08-28
LIAISON TOXO IGM II, LIAISON CONTROL TOXO IGM II (K131441)DiaSorin, Inc.2013-08-09
VIDAS TOXO IGG AVIDITY (K101946)bioMerieux, Inc.2011-05-18
ADVIA CENTAUR TOXOPLASMA IGG (TOXO G) (K102681)Siemens Healthcare Diagnostics, Inc.2011-05-04
PLATELIA TOXO IGM KIT MODEL 26211 (K090847)Bio-Rad Laboratories2009-07-01
ROCHE ELECSYS TOXO IGG TEST SYSTEM, ROCHE ELECSYS PRECICONTROL TOXO IGG (K073501)Roche Diagnostics Corp.2008-06-09

Recalls involving this device

No recalls on record reference this clearance.