ActivSight Intraoperative Imaging System— 510(k) K203550
Substantially EquivalentActiv Surgical, Inc.
FDA 510(k) clearance K203550 for ActivSight Intraoperative Imaging System, Substantially Equivalent on 2021-04-08. Applicant: Activ Surgical, Inc..
Clearance details
- Applicant
- Activ Surgical, Inc.
- Product code
- Code OWN
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Boston, MA, US
Adverse events under product code OWN
product code OWN- Malfunction
- 1,286
- Total
- 1,286
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.