FIBERFILL SGP— 510(k) K023819
Substantially EquivalentPentron Clinical Technologies
FDA 510(k) clearance K023819 for FIBERFILL SGP, Substantially Equivalent on 2003-03-26. Applicant: Pentron Clinical Technologies.
Clearance details
- Applicant
- Pentron Clinical Technologies
- Product code
- Code EKM
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wallingford, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.