Heart Technology Mfg., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Heart Technology Mfg., Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Heart Technology Mfg., Inc. has 3 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 3 cleared submissions from 1995 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Heart Technology Mfg., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Heart Technology Mfg., Inc.
3 devices
Cleared
Apr 25, 1996
ROTABLATOR SYSTEM'S GUIDE WIRE LINE: SUPPORT ROTAWIRE RAIL ROTA WIRE
Cardiovascular
90d
Cleared
Jan 18, 1996
ROTABLATOR ROTATIONAL ANGIOPLASTY SYSTEM ROTABLATOR SYSTEM'S GUIDE WIRE LINE
Cardiovascular
106d
Cleared
Dec 22, 1995
ROTABLATOR ROTATIONAL ANGIOPLASTY
Cardiovascular
120d