MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V— 510(k) K033657
Substantially EquivalentLiving Data Technologies Corporation
FDA 510(k) clearance K033657 for MOBILE EXTERNAL COUNTER PULSATION SYSTEM ANGIONEW-V, Substantially Equivalent on 2003-12-19. Applicant: Living Data Technologies Corporation.
Clearance details
- Applicant
- Living Data Technologies Corporation
- Product code
- Code DRN
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Great Neck, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.