Atlas FDA

EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY

FDA 510(k) clearance K053061 · decided 2006-02-06

Clearance details

K-number
K053061
Device name
EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY
Applicant
Dade Behring, Inc.
Decision
Substantially Equivalent
Date received
2005-10-31
Decision date
2006-02-06
Days to decision
98 days
Clearance type
Traditional
Product code
MKW
Device class
2
Regulation number
862.1235
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Newark, DE, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Dade Behring

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
ARCHITECT CYCLOSPORINE (K080751)Fujirebio Diagnostics,Inc.2008-09-11
ADVIA CENTAUR CYCLOSPORINE ASSAY AND CALIBRATOR (K071455)Siemens Medical Solutions Diagnostics2008-09-11
DIMENSION VISTA CSAE FLEX REGENT CARTRIDGE, MODEL K4108 (K081992)Siemens Healthcare Diagnostics, Inc.2008-08-05
DIMENSION VISTA CYCLOSPORINE (CSA) FLEX REAGENT CARTRIDGE (K062236)Dade Behring, Inc.2006-08-21
CYCLOSPORINE EXTENDED RANGE ASSAY (CSAE) FLEX REAGENT CARTRIDGE, CATALOG # DF108 (K052017)Dade Behring, Inc.2005-09-01
AXSYM CYCLOSPORINE (K040761)Abbott Laboratories, Inc.2004-04-30
CEDIA CYCLOSPORINE PLUS ASSAY (K023208)Microgenics Corp.2002-10-24
CYCLOSPORINE (CSA) FLEX REAGENT CARTRIDGE (K023065)Dade Behring, Inc.2002-10-16

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
COBAS INTEGRA 400 PLUS CYCLOSPORINE (P920031/S003)Dade Behring, Inc.2002-07-24
COBAS INTEGRA CYCLOSPORINE (P920031/S002)Dade Behring, Inc.2002-02-26
EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY (P920031/S001)Dade Behring, Inc.2000-08-11
EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY (P920031)Dade Behring, Inc.1996-10-02