SONOPSY LA SYSTEM— 510(k) K980423

Substantially Equivalent

Neovision Corp.

FDA 510(k) clearance K980423 for SONOPSY LA SYSTEM, Substantially Equivalent on 1998-08-07. Applicant: Neovision Corp..

Clearance details

Applicant: Neovision Corp.
Product code: Code IYO
Advisory panel: Radiology
Date received: 1998-02-03
Decision date: 1998-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwalk, CT, 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.