9150A, 1100F— 510(k) K932355

Substantially Equivalent

Dynarad Corp.

FDA 510(k) clearance K932355 for 9150A, 1100F, Substantially Equivalent on 1993-08-03. Applicant: Dynarad Corp..

Clearance details

Applicant: Dynarad Corp.
Product code: Code IZL
Advisory panel: Radiology
Date received: 1993-05-13
Decision date: 1993-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Deer Park, NY, US

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Adverse events under product code IZL

product code IZL

Other: 3
Total: 3

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.