FILMARRAY RP PANEL— 510(k) K120267
Substantially EquivalentIdaho Technology, Inc.
FDA 510(k) clearance K120267 for FILMARRAY RP PANEL, Substantially Equivalent on 2012-05-15. Applicant: Idaho Technology, Inc..
Clearance details
- Applicant
- Idaho Technology, Inc.
- Product code
- Code OCC
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Adverse events under product code OCC
product code OCC- Death
- 3
- Malfunction
- 706
- Total
- 709
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.