EROJECT, MINIJECT, SELF ASPIRATING SYRINGES, ASPIRATING SYRINGES, NON ASPIRATING SYRINGES— 510(k) K040671

Name: FDA 510(k) clearance K040671
Creator: U.S. Food and Drug Administration
Published: 2004-12-14

Substantially Equivalent

Anthogyr

FDA 510(k) clearance K040671 for EROJECT, MINIJECT, SELF ASPIRATING SYRINGES, ASPIRATING SYRINGES, NON ASPIRATING SYRINGES, Substantially Equivalent on 2004-12-14. Applicant: Anthogyr. Device class: 2.

Clearance details

Applicant: Anthogyr
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 2004-03-15
Decision date: 2004-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

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