HYPODERMIC JET INJECTION APPARATUS— 510(k) K962017

Name: FDA 510(k) clearance K962017
Creator: U.S. Food and Drug Administration
Published: 1996-07-26

Substantially Equivalent

American Jet Injector Corp.

FDA 510(k) clearance K962017 for HYPODERMIC JET INJECTION APPARATUS, Substantially Equivalent on 1996-07-26. Applicant: American Jet Injector Corp.. Device class: 2.

Clearance details

Applicant: American Jet Injector Corp.
Product code: Code EGM
Device class: Class 2
Regulation: 21 CFR 872.4475
Advisory panel: Dental
Date received: 1996-05-23
Decision date: 1996-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lansdale, PA, 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.