TETRAD MODEL 6F, END-VIEWING, ENDOCAVITY PROBE, 4.5/8.5 MHZ, CA— 510(k) K945318

Substantially Equivalent

Tetra Corp.

FDA 510(k) clearance K945318 for TETRAD MODEL 6F, END-VIEWING, ENDOCAVITY PROBE, 4.5/8.5 MHZ, CA, Substantially Equivalent on 1995-05-05. Applicant: Tetra Corp..

Clearance details

Applicant: Tetra Corp.
Product code: Code ITX
Advisory panel: Radiology
Date received: 1994-11-01
Decision date: 1995-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Englewood, CO, 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.