Tetra Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Tetra Corp. makes
Tetra Corp. makes ultrasound imaging systems and transducers, including the Tetrad 2300 E/U ultrasound imaging system and the Tetrad Model 6F end-viewing, endocavity probe operating at 4.5/8.5 MHz. The company also produces endosurgical needle guide attachments such as the Tetrad Model BS18 and automatic biopsy units like the Tetrad Model BG22.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. Tetra Corp. is based in the United States.
Catalogue
New Ultrasound Imaging System & Transducers Ref K924204
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Tetrad 2300 E/U Ultrasoung Imaging System Ref K946277
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Tetrad Model BG22, Automatic Biopsy Unit Model Ref K945320
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tetra Corp. have in the registry?
The registry currently lists 5 devices for Tetra Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tetra Corp.'s devices?
Among its 5 most recently registered devices, Tetra Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Tetra Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Tetra Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tetra Corp. in the registry?
The most recently registered devices listed for Tetra Corp. include NEW ULTRASOUND IMAGING SYSTEM & TRANSDUCERS, TETRAD MODEL BS18, ENDOSURGICAL NEEDLE GUIDE ATTACHMENT, TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM and TETRAD MODEL 6F, END-VIEWING, ENDOCAVITY PROBE, 4.5/8.5 MHZ, CA.