CARDIOTHORACIC RULER— 510(k) K902378

Substantially Equivalent

Devcom, Inc.

FDA 510(k) clearance K902378 for CARDIOTHORACIC RULER, Substantially Equivalent on 1990-06-14. Applicant: Devcom, Inc..

Clearance details

Applicant: Devcom, Inc.
Product code: Code KPR
Advisory panel: Radiology
Date received: 1990-05-29
Decision date: 1990-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, US

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Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.