Medical Device Manufacturer · US , San Jose , CA

Tetra Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1993

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Tetra Corp. Radiology ✕

5 devices

1-5 of 5

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