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.. Device class: 2.
Clearance details
- Applicant
- Heartforce Medical, Inc.
- Product code
- Code DXR
- Device class
- Class 2
- Regulation
- 21 CFR 870.2320
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Appollo Beach, FL, US
Recent devices under product code DXR
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