MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL— 510(k) K901952
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K901952 for MAG RESON DIAG DEV ACCESS SPEC PURP REC ONLY COIL, Substantially Equivalent on 1990-08-17. Applicant: Siemens Medical Solutions USA, Inc..
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code LNH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Iselin, NJ, US
Adverse events under product code LNH
product code LNH- Death
- 11
- Injury
- 670
- Malfunction
- 1,460
- Other
- 2
- Total
- 2,143
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.