DURAFLOR— 510(k) K961893

Substantially Equivalent

Pharmascience, Inc.

FDA 510(k) clearance K961893 for DURAFLOR, Substantially Equivalent on 1996-08-14. Applicant: Pharmascience, Inc.. Device class: 2.

Clearance details

Applicant: Pharmascience, Inc.
Product code: Code LBH
Device class: Class 2
Regulation: 21 CFR 872.3260
Advisory panel: Dental
Date received: 1996-05-16
Decision date: 1996-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Severn, MD, US

Download summary PDF View on FDA.gov ↗

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