MTX GENERATOR— 510(k) K880352

Substantially Equivalent

Philips Medical Systems (Cleveland), Inc.

FDA 510(k) clearance K880352 for MTX GENERATOR, Substantially Equivalent on 1988-07-14. Applicant: Philips Medical Systems (Cleveland), Inc..

Clearance details

Applicant: Philips Medical Systems (Cleveland), Inc.
Product code: Code KPR
Advisory panel: Radiology
Date received: 1988-01-26
Decision date: 1988-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Highland Heights, OH, US

Download summary PDF View on FDA.gov ↗

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.