RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES— 510(k) K885211

Substantially Equivalent

Rf Design Assoc., Inc.

FDA 510(k) clearance K885211 for RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES, Substantially Equivalent on 1989-06-13. Applicant: Rf Design Assoc., Inc..

Clearance details

Applicant: Rf Design Assoc., Inc.
Product code: Code IYN
Advisory panel: Radiology
Date received: 1988-12-14
Decision date: 1989-06-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plano, TX, US

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Adverse events under product code IYN

product code IYN

Death: 25
Injury: 163
Malfunction: 1,538
Other: 4
Total: 1,730

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.