Mansfield Scientific, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mansfield Scientific, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Mansfield Scientific, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 8 cleared submissions from 1984 to 1987. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Mansfield Scientific, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mansfield Scientific, Inc.
8 devices
Cleared
Dec 15, 1987
ANGIOSCOPE
Cardiovascular
357d
Cleared
Feb 20, 1987
ENDOMYOCARDIAL BIOPSY DEVICE
Cardiovascular
35d
Cleared
Feb 18, 1986
CIRIBART GYUDUBG CATGETER
Cardiovascular
57d
Cleared
Dec 04, 1985
EXPLORER
Cardiovascular
79d
Cleared
Sep 16, 1985
HEPARIN COAT TRAN BALLO TIP TEMP PAC ELECTRODE
Cardiovascular
80d
Cleared
Jul 19, 1985
PERCUTANEOUS TRANSLUMINAL BLOOD DILATION CATHETER
Cardiovascular
84d
Cleared
Jan 02, 1985
TRANSVENOUS BALLOON TIPPED(FLOW DIRECTED) TEMP. PA
Cardiovascular
27d
Cleared
Jul 13, 1984
WEDGE PRESSURE CATHETER FLOW DIRECTED
Cardiovascular
81d