LIMELIGHT— 510(k) K953079

Substantially Equivalent

Pulpdent Corp.

FDA 510(k) clearance K953079 for LIMELIGHT, Substantially Equivalent on 1995-08-07. Applicant: Pulpdent Corp..

Clearance details

Applicant: Pulpdent Corp.
Product code: Code EJK
Advisory panel: Dental
Date received: 1995-07-03
Decision date: 1995-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Watertown, MA, US

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