EUROFLEX F-IV, ISOFLEX III— 510(k) K863007
Substantially EquivalentSds Dental, Inc.
FDA 510(k) clearance K863007 for EUROFLEX F-IV, ISOFLEX III, Substantially Equivalent on 1986-10-01. Applicant: Sds Dental, Inc..
Clearance details
- Applicant
- Sds Dental, Inc.
- Advisory panel
- Unknown
- 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.