Hemocue, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hemocue, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Hemocue, Inc. has 9 FDA 510(k) cleared medical devices. Based in Potomac, US.
Historical record: 9 cleared submissions from 1991 to 2004. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Hemocue, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hemocue, Inc.
9 devices
Cleared
Jun 10, 2004
HEMOCUE HEMOGLOBIN 201DM ANALYZING SYSTEM
Hematology
31d
Cleared
May 20, 2004
CLINICAL LABORATORY ANALYZING SYSTEM
Chemistry
10d
Cleared
Aug 25, 2003
HEMOCUE HEMOGLOBIN 201 + SYSTEM ARTICLE 121704
Hematology
38d
Cleared
Apr 03, 2002
HEMOCUE GLUCOSE 201 SYSTEM, ARTICLE NUMBER 120706
Chemistry
12d
Cleared
Oct 15, 1996
HEMOCUE B-GLCOSE SYSTEM
Chemistry
125d
Cleared
Sep 24, 1996
HEMOCUE B-HEMOGLOBIN SYSTEM
Hematology
173d
Cleared
Aug 23, 1996
HEMOCUE B-GLUCOSE SYSTEM
Chemistry
141d
Cleared
Jan 17, 1995
HEMOCUE B-GLUCOSE SYSTEM
Chemistry
186d
Cleared
May 08, 1991
HEMOCUE(R) B-GLUCOSE MICROCUVETTE/PHOTOMETER
Chemistry
55d