EndoTool SubQ 2.1— 510(k) K211160
Substantially EquivalentMonarch Medical Technologies, LLC
FDA 510(k) clearance K211160 for EndoTool SubQ 2.1, Substantially Equivalent on 2021-10-28. Applicant: Monarch Medical Technologies, LLC.
Clearance details
- Applicant
- Monarch Medical Technologies, LLC
- Product code
- Code NDC
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Charlotte, NC, US
Adverse events under product code NDC
product code NDC- Malfunction
- 1,390
- Total
- 1,390
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.