HU-FRIEDY DENTAL CARTRIDGE SYRINGE— 510(k) K120659

Name: FDA 510(k) clearance K120659
Creator: U.S. Food and Drug Administration
Published: 2012-11-06

Substantially Equivalent

Hu-Friedy Mfg. Co., LLC

FDA 510(k) clearance K120659 for HU-FRIEDY DENTAL CARTRIDGE SYRINGE, Substantially Equivalent on 2012-11-06. Applicant: Hu-Friedy Mfg. Co., LLC. Device class: 2.

Clearance details

Applicant: Hu-Friedy Mfg. Co., LLC
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 2012-03-05
Decision date: 2012-11-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, 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.