ADMS MULTIPLANE RECTAL PROBE— 510(k) K895359

Substantially Equivalent

Avalon Technology Corp.

FDA 510(k) clearance K895359 for ADMS MULTIPLANE RECTAL PROBE, Substantially Equivalent on 1989-11-22. Applicant: Avalon Technology Corp..

Clearance details

Applicant: Avalon Technology Corp.
Product code: Code ITX
Advisory panel: Radiology
Date received: 1989-08-28
Decision date: 1989-11-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.