Interson Corp.
Interson Corp. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1991.
Top product codes for Interson Corp.
Recent clearances by Interson Corp.
- K911116 — INTERSON ENDOCAVITY PROBE/KONTRON ULTRASOUND SYST
- K911113 — INTERSON TRANSRECTAL PROBE/KONTRON ULTRASOUND SYST
- K911115 — INTERSON TRANSRECTAL PROBE/ATL ULTRASOUND SYSTEM
- K911117 — INTERSON ENDOCAVITY PROBE FOR ATL ULTRASOUND SYST
- K911114 — INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM
- K911464 — INTERSON DISPOSABLE BIOPSY NEEDLE
- K900555 — INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.
- K896680 — PROBE SHEATH FOR ADMS & CAPISTRANO LABS TRANSREC.
- K895725 — BIOPSY NEEDLE GUIDE FOR ADMS ULTRASOUND PROBES
Data sourced from openFDA. This site is unofficial and independent of the FDA.