SERIES V-SCAN RADIOGRAPHIC FILM SCANNER— 510(k) K925664

Substantially Equivalent

Vision Ten, Inc.

FDA 510(k) clearance K925664 for SERIES V-SCAN RADIOGRAPHIC FILM SCANNER, Substantially Equivalent on 1993-06-22. Applicant: Vision Ten, Inc..

Clearance details

Applicant: Vision Ten, Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 1992-11-10
Decision date: 1993-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Torrance, CA, US

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.