IRIS Thermocoagulator and Digital Colposcope— 510(k) K202915
Substantially EquivalentLiger Medical, LLC
FDA 510(k) clearance K202915 for IRIS Thermocoagulator and Digital Colposcope, Substantially Equivalent on 2021-04-23. Applicant: Liger Medical, LLC.
Clearance details
- Applicant
- Liger Medical, LLC
- Product code
- Code HGI
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lehi, UT, US
Adverse events under product code HGI
product code HGI- Other
- 1
- Total
- 1
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.