K882177

Substantially Equivalent

ADD-ON TO CRITICAL PATIENT CARE BED

Applicant: Cardio Systems, Inc.
Product code: IOQ
Advisory panel: Physical Medicine
Date received: 1988-05-24
Decision date: 1988-12-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

Adverse events under product code IOQ

product code IOQ

Malfunction: 676
Other: 5
Total: 681

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.