DIASONICS SPA 3.5 MHZ, 30MM PROBE— 510(k) K864812

Name: FDA 510(k) clearance K864812
Creator: U.S. Food and Drug Administration
Published: 1987-03-10

Substantially Equivalent

Diasonics, Inc.

FDA 510(k) clearance K864812 for DIASONICS SPA 3.5 MHZ, 30MM PROBE, Substantially Equivalent on 1987-03-10. Applicant: Diasonics, Inc.. Device class: 2.

Clearance details

Applicant: Diasonics, Inc.
Product code: Code ITX
Device class: Class 2
Regulation: 21 CFR 892.1570
Advisory panel: Radiology
Date received: 1986-12-09
Decision date: 1987-03-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milipitas, CA, US

Download summary PDF View on FDA.gov ↗

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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.