CENTRIX NEEDLETUBE— 510(k) K882651

Substantially Equivalent

Centrix, Inc.

FDA 510(k) clearance K882651 for CENTRIX NEEDLETUBE, Substantially Equivalent on 1988-08-10. Applicant: Centrix, Inc..

Clearance details

Applicant: Centrix, Inc.
Product code: Code EKJ
Advisory panel: Dental
Date received: 1988-06-27
Decision date: 1988-08-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milford, CT, US

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