THE X-RAY DIGITIZER, ALTEK MODEL ACT20020-BL— 510(k) K895442
Substantially EquivalentAltek Corp.
FDA 510(k) clearance K895442 for THE X-RAY DIGITIZER, ALTEK MODEL ACT20020-BL, Substantially Equivalent on 1989-12-14. Applicant: Altek Corp..
Clearance details
- Applicant
- Altek Corp.
- Product code
- Code KPQ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Silver Spring, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.