DIGITAL RADIOGRAPHY CHEST DEVICE— 510(k) K803049

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K803049 for DIGITAL RADIOGRAPHY CHEST DEVICE, Substantially Equivalent on 1981-03-02. Applicant: Philips Medical Systems (Cleveland), Inc..

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPR
Advisory panel: Radiology
Date received: 1980-12-01
Decision date: 1981-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.