Resonance Innovations, LLC
Omaha, NE, US
Resonance Innovations, LLC appears in FDA device records in Omaha, NE. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Resonance Innovations, LLC between 2006 and 2014. The busiest year on record is 2014, with 5. The most recent is 2014, with 5.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2006 | 2 |
| 2013 | 1 |
| 2014 | 5 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K142676 | Siemens 3.0T PROCURE Array Coil | MOS | Substantially Equivalent | |
| K142755 | Siemens 3.0 Blanket Array Coil | MOS | Substantially Equivalent | |
| K140606 | 1.5T PROCURE ARRAY COIL, 3.0T PROCURE ARRAY COIL | MOS | Substantially Equivalent | |
| K140282 | ST SENSE NV 8 ARRAY COIL | MOS | Substantially Equivalent | |
| K133986 | 1.5T ORBIT AND MANDIBLE ARRAY, 3.0T ORBIT AND MANDIBLE ARRAY | MOS | Substantially Equivalent | |
| K130457 | 3T DISTAL COIL, 3T ELBOW COIL, 3T LONG BONE COIL | MOS | Substantially Equivalent | |
| K061170 | 3.0T PEDIATRIC HEAD AND SPINE ARRAY, MODEL 808GE3000 | MOS | Substantially Equivalent | |
| K060689 | 1.5T PEDIATRIC HEAD AND SPINE ARRAY MODEL | MOS | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain