AUROFLUID 22— 510(k) K970044

Substantially Equivalent

Metalor Dental USA Corp.

FDA 510(k) clearance K970044 for AUROFLUID 22, Substantially Equivalent on 1997-03-05. Applicant: Metalor Dental USA Corp..

Clearance details

Applicant: Metalor Dental USA Corp.
Product code: Code EJS
Advisory panel: Dental
Date received: 1997-01-06
Decision date: 1997-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleborough, MA, US

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