Tetra Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K946277 | TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM | IYN | 1996-03-15 | View |
| 510(k) | K945320 | TETRAD MODEL BG22, AUTOMATIC BIOPSY UNIT MODEL | ITX | 1995-05-11 | View |
| 510(k) | K945318 | TETRAD MODEL 6F, END-VIEWING, ENDOCAVITY PROBE, 4.5/8.5 MHZ, CA | ITX | 1995-05-05 | View |
| 510(k) | K945319 | TETRAD MODEL BS18, ENDOSURGICAL NEEDLE GUIDE ATTACHMENT | ITX | 1995-05-04 | View |
| 510(k) | K924204 | NEW ULTRASOUND IMAGING SYSTEM & TRANSDUCERS | IYN | 1993-06-07 | View |
No matching devices.
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