VITAPEX PRE-LOADED DENTAL SYRINGE— 510(k) K973667

Name: FDA 510(k) clearance K973667
Creator: U.S. Food and Drug Administration
Published: 1997-11-06

Substantially Equivalent

Neodental Chemical Products Co., Ltd.

FDA 510(k) clearance K973667 for VITAPEX PRE-LOADED DENTAL SYRINGE, Substantially Equivalent on 1997-11-06. Applicant: Neodental Chemical Products Co., Ltd.. Device class: 2.

Clearance details

Applicant: Neodental Chemical Products Co., Ltd.
Product code: Code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 1997-09-25
Decision date: 1997-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethesda, MD, US

Download summary PDF View on FDA.gov ↗

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