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OLYMPUS D-DIMER REAGENT, MODEL OSR6X135, OLYMPUS D-DIMER CALIBRATOR, MODEL ODR3033, OLYMPUS D-DIMER CONTROL

FDA 510(k) clearance K070453 · decided 2007-06-11

Clearance details

K-number
K070453
Device name
OLYMPUS D-DIMER REAGENT, MODEL OSR6X135, OLYMPUS D-DIMER CALIBRATOR, MODEL ODR3033, OLYMPUS D-DIMER CONTROL
Applicant
Olympus Life & Material Science Europa GmbH (Irish
Decision
Substantially Equivalent
Date received
2007-02-16
Decision date
2007-06-11
Days to decision
115 days
Clearance type
Traditional
Product code
GHH
Device class
2
Regulation number
864.7320
Medical specialty
Hematology
Advisory committee
Hematology
Location
Irving, TX, US
Third-party review
No
Expedited review
No

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RecordFirmDate
DIAZYME D-DIMER ASSAY KIT,CALIBRATOR SETAND CONTROL SET (K112120)Diazyme Laboratories2013-01-24
PATHFAST D-DIMER (K072288)Mitsubishi Kagaku Iatron2009-05-06
TINA-QUANT D-DIMER TEST SYSTEM (K062203)Roche Diagnostics Corp.2007-03-14
TRIAGE D-DIMER TEST, MODEL 98100 (K042890)Biosite Incorporated2004-11-29
MODIFICATION TO TINA-QUANT D-DIMER TEST SYSTEM (K030740)Roche Diagnostics Corp.2003-04-01
MDA D-DIMER (K021877)bioMerieux, Inc.2002-08-07
TINA-QUANT D-DIMER TEST SYSTEM (K011143)Roche Diagnostics Corp.2001-05-29
SIMPLIFY D-DIMER, MODEL DCGK1 (K993276)Agen Biomedical , Ltd.1999-12-14
OPUS D-DIMER (K972316)Behring Diagnostics, Inc.1997-09-09
AGEN DIMERTEST GOLD EIA (K945642)Agen Biomedical , Ltd.1995-10-25
FDP - SLIDEX DIRECT (K921989)Biomerieux Vitek, Inc.1993-11-03
MINUTEX D-DIMER LATEX TEST (K920668)Biopool AB1992-10-16

Recalls involving this device

No recalls on record reference this clearance.