Atlas FDA

IL TEST CHOLINESTERASE

FDA 510(k) clearance K943367 · decided 1996-02-05

Clearance details

K-number
K943367
Device name
IL TEST CHOLINESTERASE
Applicant
Instrumentation Laboratory CO
Decision
Substantially Equivalent
Date received
1994-07-13
Decision date
1996-02-05
Days to decision
572 days
Clearance type
Traditional
Product code
DIH
Device class
1
Regulation number
862.3240
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Lexington, MA, 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
SYNCHRON SYSTEMS CHOLINESTERASE (CHEX) MODEL A53722 (K103373)Beckman Coulter, Inc.2011-02-07
CHOLINESTERASE GEN.2 TEST SYSTEM (K061093)Roche Diagnostics Corp.2006-07-03
SENTINEL CHOLINESTERASE LIQUID (K051444)Sentinel Ch. Srl2005-06-20
OLYMPUS CHOLINESTERASE REAGENT (CATALOG NUMBER OSR6114) (K030045)Olympus America, Inc.2003-02-21
WIENER LAB COLINESTERASA AA (K023992)Wiener Laboratories Saic2003-02-12
ADVIA 1650 CHOLINESTERASE ASSAY (K013750)Bayer Diagnostics Corp.2002-01-18
CARESIDE CHOLINESTERASE (K002792)Careside, Inc.2000-11-08
ADVIA IMS (K001344)Bayer Corp.2000-06-26
TEST-MATE CHE CHOLINESTERASE TEST SYSTEM (K961656)Eqm Research, Inc.1996-11-26
CHOLINESTERASE ASSAY KIT, CATALOGUE# 300-05 (K955498)Diagnostic Chemicals , Ltd.1996-01-24
IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE (K914171)Tech Intl. Co.1991-12-18
KODAK EKTACHEM DT SLIDES (CHE) (K913198)Eastman Kodak Company1991-08-26

Recalls involving this device

No recalls on record reference this clearance.