Tronomed, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Tronomed, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1977 to 1996. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tronomed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tronomed, Inc.
12 devices
Cleared
Jan 11, 1996
TRONOMATE PATIENT CABLE & LEADWIRE SYSTEM
Cardiovascular
213d
Cleared
Sep 18, 1985
LIFELINC LEADWIRE
Anesthesiology
43d
Cleared
Sep 10, 1985
LIFE LINC PATIENT CABLE
Anesthesiology
25d
Cleared
Jul 24, 1985
HIGH PRESSURE FLEX. CONNECTING TUBING
Cardiovascular
498d
Cleared
Jan 16, 1980
TANDEM ASSEMBLED 3&4 WAY STOPCOCKS
General Hospital
84d
Cleared
Jan 16, 1980
3&4 WAY PLASTIC STOPCOCKS, NONSTERILE
General Hospital
84d
Cleared
Jan 16, 1980
3&4 WAY PLASTIC STERILE STPCKS. PKG.
General Hospital
84d
Cleared
Jan 16, 1980
PLAS. STCK. W/EXTENSION TUBE/STERILE
General Hospital
84d
Cleared
Jan 16, 1980
STERILE EXTENSION TUBES INDIV. PKG.
General Hospital
84d
Cleared
Oct 18, 1977
ELECTROCARDIOGRAPHIC CABLHS & LEAD WIRE
Cardiovascular
50d
Cleared
Jul 05, 1977
ELECTROCARDIOGRAPHIC PATIENT CABLES
Cardiovascular
27d
Cleared
May 23, 1977
ELHCTROCARDIOGRAPHIC CONNECTING WIRES
Cardiovascular
7d