PRESTYL JET INJECTOR— 510(k) K922683

Substantially Equivalent

Bma Technologies S.A.

FDA 510(k) clearance K922683 for PRESTYL JET INJECTOR, Substantially Equivalent on 1994-04-11. Applicant: Bma Technologies S.A.. Device class: 2.

Clearance details

Applicant: Bma Technologies S.A.
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 1992-06-04
Decision date: 1994-04-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJI

K171254 — LeEject 2 Dental Syringe and Needle System2017-11-16
K142414 — Miltex N-Tralig Intraligamentary Syringe2014-10-30
K120659 — HU-FRIEDY DENTAL CARTRIDGE SYRINGE2012-11-06
K113247 — ANESTHESIA INJECTION TOOL SET2012-03-27
K082249 — MORPHEUS2009-12-31

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