REVISED T-SCAN SYSTEM— 510(k) K870032
Substantially EquivalentSentek, Inc.
FDA 510(k) clearance K870032 for REVISED T-SCAN SYSTEM, Substantially Equivalent on 1987-02-02. Applicant: Sentek, Inc..
Clearance details
- Applicant
- Sentek, Inc.
- Product code
- Code EFH
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.