SANKO INTRAORAL DENTAL X-RAY— 510(k) K972921
Substantially EquivalentSanko X-Ray Manufacturing Co., Ltd.
FDA 510(k) clearance K972921 for SANKO INTRAORAL DENTAL X-RAY, Substantially Equivalent on 1998-01-06. Applicant: Sanko X-Ray Manufacturing Co., Ltd..
Clearance details
- Applicant
- Sanko X-Ray Manufacturing Co., Ltd.
- Product code
- Code EHD
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Virginia Beach, VA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.