VERTEX DIGITAL SUBSTRATION KIT— 510(k) K830637
Substantially EquivalentProfessional Medical Services
FDA 510(k) clearance K830637 for VERTEX DIGITAL SUBSTRATION KIT, Substantially Equivalent on 1983-03-24. Applicant: Professional Medical Services.
Clearance details
- Applicant
- Professional Medical Services
- Product code
- Code DQO
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Adverse events under product code DQO
product code DQO- Death
- 35
- Injury
- 993
- Malfunction
- 1,772
- Other
- 5
- Total
- 2,805
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.