MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE— 510(k) K843314

Name: FDA 510(k) clearance K843314
Creator: U.S. Food and Drug Administration
Published: 1984-09-27

Substantially Equivalent

Smith & Nephew, Mpl Division

FDA 510(k) clearance K843314 for MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE, Substantially Equivalent on 1984-09-27. Applicant: Smith & Nephew, Mpl Division. Device class: 2.

Clearance details

Applicant: Smith & Nephew, Mpl Division
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 1984-08-24
Decision date: 1984-09-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EJI

view all

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

More clearances from Smith & Nephew, Mpl Division

view all

K841280 — SOLOPAK BRAND FILTER NEEDLE W/5 MICRO1984-05-21
K840237 — MAX-I-PROBE PERIODONTAL ENDODONTIC PROB1984-04-05
K833304 — HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST1984-03-30
K832126 — MICRO Z DISPOS. SPINAL ANESTH. NEEDLE1983-08-12
K831765 — HERAPIN LOCK FLUSH SOLUTION USE KIT1983-07-12

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