VASOVIEW DUPLEX IMAGING SYSTEM— 510(k) K861237

Substantially Equivalent for Some Indications

Sonicaid, Inc.

FDA 510(k) clearance K861237 for VASOVIEW DUPLEX IMAGING SYSTEM, Substantially Equivalent for Some Indications on 1986-07-14. Applicant: Sonicaid, Inc..

Clearance details

Applicant: Sonicaid, Inc.
Product code: Code ITX
Advisory panel: Radiology
Date received: 1986-04-02
Decision date: 1986-07-14
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Fredericksburg, VA, US

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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.