• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
128 records meeting your search criteria returned- Product Code: LCP Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SIEMENS HEALTHCARE DIAGNOSTICS INC. DIMENSION® 04/29/2019
ROCHE DIAGNOSTICS COBAS B 101 HBA1C TEST 02/21/2019
ROCHE DIAGNOSTICS COBAS B 101 HBA1C TEST 10/01/2018
ROCHE DIAGNOSTICS COBAS B 101 HBA1C TEST 09/11/2018
ROCHE DIAGNOSTICS COBAS B 101 HBA1C TEST 07/12/2018
ROCHE DIAGNOSTICS HBA1C III TINA-QUANT HEMOGLOBIN A1C III 05/22/2018
TOSOH CORPORATION TOSOH HLC-723G8 ANALYZER G8 03/15/2018
ROCHE DIAGNOSTICS COBAS INTEGRA (800) HBA1CDX GEN 2 01/17/2018
BECKMAN COULTER BECKMAN COULTER AU480 01/11/2018
ROCHE DIAGNOSTICS COBAS 6000 C501 MODULE 01/11/2018
-
-