CEROX MODEL 3210— 510(k) K093923
Substantially EquivalentOr-Nim Medical , Ltd.
FDA 510(k) clearance K093923 for CEROX MODEL 3210, Substantially Equivalent on 2010-01-19. Applicant: Or-Nim Medical , Ltd..
Clearance details
- Applicant
- Or-Nim Medical , Ltd.
- Product code
- Code MUD
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Lod, IL
Adverse events under product code MUD
product code MUD- Malfunction
- 467
- Total
- 467
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.