OsteoProbe— 510(k) DEN210013
UnknownActive Life Scientific, Inc.
FDA 510(k) clearance DEN210013 for OsteoProbe, Unknown on 2021-08-19. Applicant: Active Life Scientific, Inc..
Clearance details
- Applicant
- Active Life Scientific, Inc.
- Product code
- Code QGQ
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Santa Barbara, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.