Triangle Biomedical Sciences, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triangle Biomedical Sciences, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Triangle Biomedical Sciences, Inc. has 6 FDA 510(k) cleared medical devices. Based in Palm Beach Gardens, US.
Historical record: 6 cleared submissions from 1996 to 1998. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Triangle Biomedical Sciences, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Triangle Biomedical Sciences, Inc.
6 devices
Cleared
Aug 07, 1998
MICRO21 WITH URINE SEDIMENT ANALYSIS
Hematology
37d
Cleared
Nov 07, 1997
MICRO21 WITH WBC ESTIMATE
Hematology
84d
Cleared
Sep 16, 1997
MICRO21 WITH CEREBROSPINAL FLUID
Hematology
147d
Cleared
Jan 03, 1997
MICRO21 WITH NDNA
Immunology
78d
Cleared
May 22, 1996
MICRO21 WITH ANA
Hematology
86d
Cleared
May 17, 1996
MICRO21 WITH RETIC
Hematology
81d