GUIDOR(TM)— 510(k) K912724

Substantially Equivalent for Some Indications

Procordia Oratech AB

FDA 510(k) clearance K912724 for GUIDOR(TM), Substantially Equivalent for Some Indications on 1993-05-13. Applicant: Procordia Oratech AB.

Clearance details

Applicant: Procordia Oratech AB
Product code: Code NPK
Advisory panel: Dental
Date received: 1991-06-18
Decision date: 1993-05-13
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Huddinge, Sweden, SE

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.