BARIREP— 510(k) K100839
Substantially EquivalentGorbec Pharmaceutical Services, Inc.
FDA 510(k) clearance K100839 for BARIREP, Substantially Equivalent on 2010-05-11. Applicant: Gorbec Pharmaceutical Services, Inc..
Clearance details
- Applicant
- Gorbec Pharmaceutical Services, Inc.
- Product code
- Code FRO
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Durham, NC, US
Adverse events under product code FRO
product code FRO- Death
- 30
- Injury
- 653
- Malfunction
- 479
- Other
- 11
- Total
- 1,173
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.