Trionix Research Laboratory, Inc. is one of 12504 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Trionix Research Laboratory, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 511 KEV COLLIMATOR, QUASAR RECOVERY IMAGING PACKAGE, CARDIAC TRIAD NUCLEAR IMAGING SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY SYSTEM
16
Total
16
Cleared
0
Denied
Trionix Research Laboratory, Inc. has 16 FDA 510(k) cleared radiology devices. Based in Twinsburg, US.
Historical record: 16 cleared submissions from 1988 to 1997.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Trionix Research Laboratory, Inc.
16 devices
Cleared
May 29, 1997
511 KEV COLLIMATOR
Radiology
205d
Cleared
Nov 27, 1996
QUASAR RECOVERY IMAGING PACKAGE
Radiology
154d
Cleared
Nov 12, 1996
CARDIAC TRIAD NUCLEAR IMAGING SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY SYSTEM
Radiology
19d
Cleared
Nov 12, 1996
BIAD NUCLEAR IMAGING SYSTEM
Radiology
19d
Cleared
Nov 12, 1996
MONAD NUCLEAR IMAGING SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY SYSTEM
Radiology
19d
Cleared
Nov 12, 1996
TRIAD 88 NUCLEAR IMAGING SYSTEM
Radiology
19d
Cleared
Sep 04, 1996
GATED MIBI 3-D EJECTION FRACTION PROCESSING
Radiology
133d
Cleared
Sep 10, 1992
CARDIAC TRIAD NEW DETECTOR OPTION
Radiology
78d
Cleared
Sep 10, 1992
BIAD NEW DETECTOR OPTION
Radiology
78d
Cleared
Aug 27, 1992
MONAD NUCLEAR IMAGING SYSTEM
Radiology
64d
Cleared
Apr 27, 1992
CARDIAC TRIAD NUCLEAR IMAGING SYSTEM
Radiology
67d
Cleared
Sep 06, 1991
ACQUPRO
Radiology
113d