ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE— 510(k) K092943

Name: FDA 510(k) clearance K092943
Creator: U.S. Food and Drug Administration
Published: 2009-12-11

Substantially Equivalent

Arnold Tuber Industries

FDA 510(k) clearance K092943 for ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE, Substantially Equivalent on 2009-12-11. Applicant: Arnold Tuber Industries. Device class: 2.

Clearance details

Applicant: Arnold Tuber Industries
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 2009-09-24
Decision date: 2009-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hamburg, NY, US

Download summary PDF View on FDA.gov ↗

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