CDR SYSTEMS PRECISION PATIENT POSITIONING SYSTEM— 510(k) K122888

Substantially Equivalent

Cdr Systems, Inc.

FDA 510(k) clearance K122888 for CDR SYSTEMS PRECISION PATIENT POSITIONING SYSTEM, Substantially Equivalent on 2013-04-30. Applicant: Cdr Systems, Inc..

Clearance details

Applicant: Cdr Systems, Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 2012-09-20
Decision date: 2013-04-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Calgary, CA

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

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.