AUGEASE VASCULAR AUGMENTATION DEVICE— 510(k) K101355
Substantially EquivalentAugdvt, LLC
FDA 510(k) clearance K101355 for AUGEASE VASCULAR AUGMENTATION DEVICE, Substantially Equivalent on 2010-10-26. Applicant: Augdvt, LLC.
Clearance details
- Applicant
- Augdvt, LLC
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.