Atlas FDA

CONTROL PLASMA P

FDA 510(k) clearance K023312 · decided 2002-11-01

Clearance details

K-number
K023312
Device name
CONTROL PLASMA P
Applicant
Dade Behring, Inc.
Decision
Substantially Equivalent
Date received
2002-10-03
Decision date
2002-11-01
Days to decision
29 days
Clearance type
Traditional
Product code
GGC
Device class
2
Regulation number
864.5425
Medical specialty
Hematology
Advisory committee
Hematology
Location
Newark, DE, 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
HEMOSIL LA POSITIVE CONTROL (K102552)Instrumentation Laboratory CO2011-04-05
SPECIALTY ASSAYED CONTROL-2 (K100103)Helena Laboratories2010-12-15
PLASMACON N, PLASMACON L-1, PLASMACON L-2 (K062306)R2 Diagnostics, Inc.2007-03-16
STA - CONTROL LA 1+2 (K061803)Diagnostica Stago, Inc.2006-07-28
CRYOCHECK WEAK LUPUS POSITIVE CONTROL (K032804)Precision Biologic2003-11-03
LYPHOCHEK HEMOSTASIS, MODELS 798, 799 (K020878)Bio-Rad2002-04-15
SIGMA DIAGNOSTICS ACCUCLOT LA CONTROL (K020109)Sigma Diagnostics, Inc.2002-02-06
K-ASSAY D-DIMER CONTROLS (K012422)Kamiya Biomedical Co.2001-08-21
SIGMA DIANOSTICS AUTO D-DIMER CONTROL LEVEL 2, MODEL A5217 (K003329)Sigma Diagnostics, Inc.2001-03-01
GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05 (K993332)Gradipore , Ltd.2000-02-16
COAGULATION CONTROL LEVEL 2 (ABNORMAL) (K984130)Pacific Hemostasis1998-12-01
COAGULATION CONTROL LEVEL 3 (ABNORMAL) (K984131)Pacific Hemostasis1998-12-01

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