MODIFICATION TO CMA CEREBRAL TISSUE MONITORING SYSTEM— 510(k) K071984
Substantially EquivalentCma Microdialysis AB
FDA 510(k) clearance K071984 for MODIFICATION TO CMA CEREBRAL TISSUE MONITORING SYSTEM, Substantially Equivalent on 2008-06-27. Applicant: Cma Microdialysis AB.
Clearance details
- Applicant
- Cma Microdialysis AB
- Product code
- Code GWM
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- North Chelmsford, MA, US
Adverse events under product code GWM
product code GWM- Death
- 21
- Injury
- 732
- Malfunction
- 2,063
- Other
- 1
- Total
- 2,817
Source: openFDA MAUDE database, through . 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.