Tetrad Corp. is one of 24547 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tetrad Corp. - FDA 510(k) Cleared Devices
Recent clearances: SONATA 3-D IMAGING ACCESSORY, MODEL 3DS, TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS, TETRAD MODEL TC-EC7-ACP, -L5-, -L7-, -V4-ACP TRANSDUCERS
4
Total
4
Cleared
0
Denied
Tetrad Corp. has 4 FDA 510(k) cleared medical devices. Based in Englewood, US.
Historical record: 4 cleared submissions from 2001 to 2004. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Tetrad Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Product Service, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tetrad Corp.
4 devices
Cleared
Dec 23, 2004
SONATA 3-D IMAGING ACCESSORY, MODEL 3DS
Radiology
87d
Cleared
Jan 03, 2002
TETRAD MODEL TC-C52-, -C84V-, -C95-, -CLA76-, -L74-ATP TRANSDUCERS
Radiology
14d
Cleared
Dec 03, 2001
TETRAD MODEL TC-EC7-ACP, -L5-, -L7-, -V4-ACP TRANSDUCERS
Radiology
13d
Cleared
May 04, 2001
TETRAD TC-C3-ACP
Radiology
288d