Reference Diagnostics, Inc. is one of 6976 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reference Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RDI HSFERRITIN KIT, FERRITIN CALIBRATOR SET, CATALOG NO. 8203, TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET
17
Total
17
Cleared
0
Denied
Reference Diagnostics, Inc. has 17 FDA 510(k) cleared chemistry devices. Based in Arlington, US.
Historical record: 17 cleared submissions from 1990 to 2006.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rdd Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Reference Diagnostics, Inc.
17 devices
Cleared
Mar 13, 2006
RDI HSFERRITIN KIT
Immunology
117d
Cleared
Mar 13, 2006
FERRITIN CALIBRATOR SET, CATALOG NO. 8203
Chemistry
108d
Cleared
Nov 09, 2005
TOTAL IRON-BINDING CAPACITY CALIBRATOR SET. DIRECT TIBC CALIBRATOR SET
Chemistry
93d
Cleared
Sep 30, 2003
EXTENDED RANGE HS CRP KIT, CAT NO:9200
Chemistry
267d
Cleared
Apr 11, 2003
RDI EXTENDED RANGE CRP CALIBRATOR SET
Immunology
31d
Cleared
Jun 27, 2002
RDI HS CRP CALIBRATOR SET
Immunology
42d
Cleared
Jun 27, 2002
RDI HS CRP KIT
Chemistry
42d
Cleared
May 04, 2000
DIRECT TIBC CALIBRATOR
Chemistry
55d
Cleared
May 02, 2000
DIRECT TIBC KIT
Chemistry
53d
Cleared
Feb 16, 1999
MAGNETIC TIBC KIT
Chemistry
25d
Cleared
Jan 28, 1999
RDI DIRECT LDL CHOLESTEROL TEST
Chemistry
72d
Cleared
Dec 22, 1997
RDI HOMOGENEOUS HDL CHOLESTEROL TEST
Chemistry
62d