133 results · 67ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DIAGNOSTIC PRODUCTS CORP. RIA CONTROL

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

IMMULITE REAGENT WEDGE

FDA Adverse Event
Injury ·DIAGNOSTIC PRODUCTS CORP·Product code JJQ·November 21, 2002

IMMULITE 2000 ANALYZER

FDA Adverse Event
DPC INSTRUMENT SYSTEMS DIVISIONS·Product code JJQ·August 11, 2003

IMMULITE 2000 ANALYZER

FDA Adverse Event
DPC INSTRUMENT SYSTEMS DIVISIONS·Product code JJQ·January 15, 2003

DIAGNOSTIC PRODUCT CORP

FDA Adverse Event
Malfunction ·*·Product code JJQ·January 23, 2006

IMMULITE 2000 INTACT PTH

FDA Adverse Event
Malfunction ·DIAGNOSTIC PRODUCTS CORP.·Product code JJQ·March 17, 2004

THIRD GENERATION TSH ASSAY

FDA Adverse Event
Malfunction ·DIAGNOSTIC PRODUCTS CORP·Product code JLW·May 16, 2006

DPC IMMULITE

FDA Adverse Event
Malfunction ·DIAGNOSTIC PRODUCTS CORP.·Product code JJE·May 3, 2004

IMMULITE 2000 H. PYLORI IGG

FDA Adverse Event
Malfunction ·DIAGNOSTIC PRODUCTS CORP.·Product code LYR·April 18, 2001

DPC IMMULITE H PYLORI IGG

FDA Adverse Event
Other ·DIAGNOSTIC PRODUCTS CORP·Product code KTO·May 8, 2001

IMMULITE 2000 Total Testosterone Kit

FDA Recall
Terminated ·Diagnostic Products Corp.·Product code CDZ·January 3, 2006

Immulite/ Immulite 1000 Carcinoembryonic Antigen (CEA) LKCE1 lot 302 and 303

FDA Recall
Terminated ·Diagnostic Products Corp·Product code DHX·May 26, 2005

Immulite 2500 insulin Kit

FDA Recall
Terminated ·Diagnostic Products Corp·Product code CFP·November 19, 2004

Immulite 2000 H. pylori IgG Kit lot 118 (L2KHQ6, 600 test size kit)

FDA Recall
Terminated ·Diagnostic Products Corp·Product code LYR·July 31, 2003

IMMULITE 2000 Intact PTH kit

FDA Recall
Terminated ·Diagnostic Products Corp·Product code CEW·February 23, 2004

Immulite 1000 CEA Catalog No. LKCE1

FDA Recall
Terminated ·Diagnostic Products Corp·Product code DHX·May 3, 2004

IMMULITE 2000 Vitamin B12 Kit, Catalog # L2KVB2, L2KVB6, kit lot 186.

FDA Recall
Terminated ·Diagnostic Products Corp·Product code CDD·January 24, 2005

DPC IMMULITE 1000

FDA Adverse Event
Malfunction ·DIAGNOSTICS PRODUCTS CORP·Product code KHO·September 13, 2004

QUATTRO PREMIER XE MASS SPECTROMETER

FDA Adverse Event
Death ·WATERS CORP·Product code OQS·March 24, 2010

LIFESYNC LEADWEAR

FDA Adverse Event
Other ·LIFESYNC CORPORATION·Product code DSA·January 9, 2009