DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300— 510(k) K081603
Substantially EquivalentHeartforce Medical, Inc.
FDA 510(k) clearance K081603 for DIGITAL BALLISTOCARDIOGRAPH, MODEL DGB 300, Substantially Equivalent on 2009-07-24. Applicant: Heartforce Medical, Inc..
Clearance details
- Applicant
- Heartforce Medical, Inc.
- Product code
- Code DXR
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Appollo Beach, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.