CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY— 510(k) K920156
Substantially EquivalentClinical Neuro Systems, LLC
FDA 510(k) clearance K920156 for CLINICAL NEURO SYST MONITORR EXT CSF DRAIN/MONI SY, Substantially Equivalent on 1992-03-16. Applicant: Clinical Neuro Systems, LLC. Device class: 2.
Clearance details
- Applicant
- Clinical Neuro Systems, LLC
- Product code
- Code JXG
- Device class
- Class 2
- Regulation
- 21 CFR 882.5550
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Goleta, CA, US
Recent devices under product code JXG
view allMore clearances from Clinical Neuro Systems, LLC
view allAdverse events under product code JXG
product code JXG- Death
- 76
- Injury
- 5,632
- Malfunction
- 2,230
- Other
- 4
- Total
- 7,942
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 →
Recalls naming K920156
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K920156.
Data sourced from openFDA. This site is unofficial and independent of the FDA.