Interson Corp.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K911116 | INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYST | ITX | 1991-12-20 | View |
| 510(k) | K911117 | INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST | ITX | 1991-12-17 | View |
| 510(k) | K911115 | INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEM | ITX | 1991-12-17 | View |
| 510(k) | K911113 | INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYST | ITX | 1991-12-17 | View |
| 510(k) | K911114 | INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM | ITX | 1991-11-19 | View |
| 510(k) | K911464 | INTERSON DISPOSABLE BIOPSY NEEDLE | IYO | 1991-09-27 | View |
| 510(k) | K900555 | INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. | ITX | 1990-05-02 | View |
| 510(k) | K896680 | PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC. | FED | 1990-02-14 | View |
| 510(k) | K895725 | BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES | FCG | 1989-11-06 | View |
No matching devices.
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