ADA-1000 (ADVANCED DIGITAL ARRAY)— 510(k) K863780

Substantially Equivalent for Some Indications

Diasonics, Inc.

FDA 510(k) clearance K863780 for ADA-1000 (ADVANCED DIGITAL ARRAY), Substantially Equivalent for Some Indications on 1986-12-29. Applicant: Diasonics, Inc..

Clearance details

Applicant: Diasonics, Inc.
Product code: Code IYO
Advisory panel: Radiology
Date received: 1986-09-26
Decision date: 1986-12-29
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Milipitas, CA, US

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Adverse events under product code IYO

product code IYO

Malfunction: 3,339
Total: 3,339

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.