Universal Reagents, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Universal Reagents, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Universal Reagents, Inc. has 8 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 8 cleared submissions from 1996 to 1997. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Universal Reagents, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Universal Reagents, Inc.
8 devices
Cleared
Sep 25, 1997
UNIVERSAL REAGENT FACTOR XII (TWELVE) DEFICIENT PLASMA
Hematology
34d
Cleared
Jul 14, 1997
FACTOR DEFICIENT PLASMAS - FACTOR XI (11)
Hematology
25d
Cleared
Jul 14, 1997
FACTOR DEFICIENT PLASMAS - FACTOR IX (9)
Hematology
25d
Cleared
Apr 25, 1997
UNIVERSAL REAGENT FACTOR VIII DEFICIENT PLASMA
Hematology
66d
Cleared
Apr 25, 1997
UNIVERSAL REAGENT FACTOR VII DEFICIENT PLASMA
Hematology
66d
Cleared
Dec 18, 1996
UNIVERSAL REAGENT FACTOR V DEFICIENT PLASMA
Hematology
54d
Cleared
Dec 18, 1996
UNIVERSAL REAGENT FACTOR X DEFICIENT PLASMA
Hematology
41d
Cleared
Oct 10, 1996
FACTOR DEFICIENT PLASMA
Hematology
146d