Tetra Corp. - FDA 510(k) Cleared Devices
Recent clearances: TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tetra Corp. Radiology ✕
5 devices
Cleared
Mar 15, 1996
TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM
Radiology
444d
Cleared
May 11, 1995
TETRAD MODEL BG22, AUTOMATIC BIOPSY UNIT MODEL
Radiology
191d
Cleared
May 05, 1995
TETRAD MODEL 6F, END-VIEWING, ENDOCAVITY PROBE, 4.5/8.5 MHZ, CA
Radiology
185d
Cleared
May 04, 1995
TETRAD MODEL BS18, ENDOSURGICAL NEEDLE GUIDE ATTACHMENT
Radiology
184d
Cleared
Jun 07, 1993
NEW ULTRASOUND IMAGING SYSTEM & TRANSDUCERS
Radiology
291d