Atlas FDA

TOXO ELISA TEST SYSTEM

FDA 510(k) clearance K891781 · decided 1989-07-14

Clearance details

K-number
K891781
Device name
TOXO ELISA TEST SYSTEM
Applicant
Zeus Scientific, Inc.
Decision
Substantially Equivalent
Date received
1989-03-24
Decision date
1989-07-14
Days to decision
112 days
Clearance type
Traditional
Product code
LGD
Device class
2
Regulation number
866.3780
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Raritan, NJ, US
Third-party review
No
Expedited review
No

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

RecordFirmDate
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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.

PMA approvals by this applicant

RecordFirmDate
ZEUS ELISA PARVOVIRUS B19 IGM TEST SYSTEM (P150042)Zeus Scientific, Inc.2017-09-19
ZEUS ELISA PARVOVIRUS B19 IGG TEST SYSTEM (P150045)Zeus Scientific, Inc.2017-09-19
FLUORO-CEP (R) PROGESTERONE (P900025/S001)Zeus Scientific, Inc.1992-04-21
FLUORO-CEP (R) PROGESTERONE (P900025/S002)Zeus Scientific, Inc.1992-04-17
FLUORO-CEP (R) PROGESTERONE (P900025)Zeus Scientific, Inc.1990-09-26